| Identifier | Protein names | Gene names | Cross reference refseq | Length | Species |
| Q16874 | Cytochrome P450 21-hydroxylase (Cytochrome P450, family 21, subfamily A, polypeptide 2, isoform CRA_b) (DJ34F7.3 (Cytochrome P450, subfamily XXIA (Steroid 21-hydroxylase, congenital adrenal hyperplasia), polypeptide 2; CYP21, P450c21B)); Steroid 21-hydrox疏?疐 | P450-CYP21B; CYP21A2; | NP_000491.4; | 495 | human |
| F2Z3Q3 | Abhydrolase domain-containing protein 16A; | ABHD16A; | NULL | 65 | human |
| Q8IUJ1 | Alpha-S2-like casein A; HCG2036852; | CSN1S2A; | NULL | 27 | human |
| B7Z385 | Adenylyl cyclase-associated protein; | CAP2; | NULL | 365 | human |
| Q7RTW5 | Neuregulin 1 isoform HRG-gamma; Neuregulin 1, isoform CRA_l; | NRG1; | NP_004486.2; | 211 | human |
| B4DJ26 | Phosphoribosylformylglycinamidine synthase (FGAR amidotransferase), isoform CRA_c; cDNA FLJ61288, highly similar to Phosphoribosylformylglycinamidine synthase (EC 6.3.5.3); | PFAS; | NULL | 914 | human |
| A0A024R330 | Chromosome 3 open reading frame 14, isoform CRA_a; | C3orf14; | NULL | 128 | human |
| A0A024R1X2 | WIRE protein, isoform CRA_a; | WIRE; | NULL | 287 | human |
| Q8NH77 | HCG2044188; Seven transmembrane helix receptor; | NULL | NULL | 288 | human |
| H9RI29 | Cytochrome c oxidase subunit 1; EC 1.9.3.1; | COX1; | NULL | 513 | human |
| A0N4X9 | HCG2039760; Possible J 30 gene segment; Fragment; | Tcr-alpha; | NULL | 18 | human |
| A0A024RDE8 | PDZ and LIM domain 5, isoform CRA_c; | PDLIM5; | NULL | 596 | human |
| F5H124 | Protein mago nashi homolog 2; | MAGOHB; | NULL | 81 | human |
| D6W5Q7 | Uncharacterized protein; | FLJ20097; | NULL | 722 | human |
| A0A024R5P1 | Phosphatidylinositol binding clathrin assembly protein, isoform CRA_i; | PICALM; | NULL | 652 | human |
| F6Q0M4 | Tumor necrosis factor receptor superfamily member 14; Fragment; | TNFRSF14; | NULL | 231 | human |
| D3DT68 | HCG1818640, isoform CRA_a; | NULL | NULL | 95 | human |
| C4P093 | Disrupted in schizophrenia 1 isoform 14; Disrupted in schizophrenia 1 isoform 18; Disrupted in schizophrenia 1 isoform 31; Disrupted in schizophrenia 1 isoform 5; Disrupted in schizophrenia 1 protein; | DISC1; | NULL | 547 | human |
| Q9NR54 | Excision repair cross-complementing rodent repair deficiency, complementation group 5, isoform CRA_b; Xeroderma pigmentosum complementation group G protein splice variant; Xeroderma pigmentosum, complementation group G (Cockayne syndrome); | ERCC5; | NULL | 67 | human |
| B4E099 | Protein DBF4 homolog B; cDNA FLJ61009, highly similar to Homo sapiens Dbf4-related factor 1 (DRF1), transcript variant 1, mRNA; | DBF4B; | NULL | 157 | human |
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