| Identifier | Protein names | Gene names | Cross reference refseq | Length | Species |
| B9EH95 | Armadillo repeat gene deletes in velocardiofacial syndrome; Armadillo repeat gene deletes in velocardiofacial syndrome, isoform CRA_b; | ARVCF; | NULL | 962 | human |
| E5E0X0 | NADH-ubiquinone oxidoreductase chain 5; EC 1.6.5.3; | ND5; | NULL | 603 | human |
| G3V0E9 | La ribonucleoprotein domain family, member 2, isoform CRA_d; La-related protein 1B; | LARP1B; LARP2; | NP_115615.2; | 358 | human |
| B5MCE7 | Basic leucine zipper and W2 domain-containing protein 2; Basic leucine zipper and W2 domains 2, isoform CRA_b; | BZW2; | NULL | 225 | human |
| G3V115 | Leucine rich repeat containing 34, isoform CRA_b; Leucine-rich repeat-containing protein 34; | LRRC34; | XP_005247190.1; | 403 | human |
| A6YUS7 | ATP synthase subunit a; | ATP6; | NULL | 226 | human |
| Q0VDG0 | PARP6 protein; Fragment; | PARP6; | NULL | 554 | human |
| Q9B2Y2 | NADH-ubiquinone oxidoreductase chain 5; EC 1.6.5.3; | ND5; | NULL | 603 | human |
| A0A087X1V8 | Ovochymase-2; | OVCH2; | NULL | 565 | human |
| B9A6J9 | Protein LOC101060376; TBC1 domain family member 3C; TBC1 domain family, member 3; | TBC1D3; LOC101060376 TBC1D3C; | NP_001278388.1; | 549 | human |
| Q2TA81 | DOK1 protein; cDNA FLJ60879, highly similar to Docking protein 1 (Downstream of tyrosinekinase 1); cDNA FLJ45754 fis, clone LYMPB2002806, highly similar to Docking protein 1 (Downstream of tyrosine kinase 1); cDNA FLJ45184 fis, highly similar to Docking p疏?疐 | DOK1; | NULL | 267 | human |
| Q496A9 | RASSF3 protein; | RASSF3; | NULL | 168 | human |
| J3KNL7 | Family with sequence similarity 63, member B, isoform CRA_d; Protein FAM63B; | FAM63B; | NULL | 422 | human |
| B5BU99 | High glucose-regulated protein 8; | YTHDF2; | NULL | 570 | human |
| Q1ET61 | Sulfotransferase; EC 2.8.2.-; | ST1A5; SULT1A3; | NP_001017390.1;NP_808220.1;XP_005276563.1;XP_005276564.1;XP_006726684.1; | 295 | human |
| Q6FH20 | NTS protein; Neurotensin, isoform CRA_b; Preproneurotensin/neuromedin N; cDNA, FLJ92347, Homo sapiens neurotensin (NTS), mRNA; | NTS; | NP_006174.1; | 170 | human |
| Q5VU50 | Bartter syndrome, infantile, with sensorineural deafness; Barttin; | BSND; | NP_476517.1; | 320 | human |
| Q53QU7 | Distal-less homeobox 2; Putative uncharacterized protein DLX2; cDNA FLJ75693, highly similar to Homo sapiens distal-less homeo box 2 (DLX2), mRNA; | DLX2; | NP_004396.1; | 328 | human |
| Q53Z07 | NPC-A-16; Ribosomal protein L9; Ribosomal protein L9 isoform; Ribosomal protein L9, isoform CRA_b; cDNA, FLJ92535, Homo sapiens ribosomal protein L9 (RPL9), mRNA; | RPL9; | NP_000652.2;NP_001020092.1;XP_005262718.1; | 192 | human |
| H3BM50 | Target of rapamycin complex subunit LST8; | MLST8; | NULL | 116 | human |
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