| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_013379.2 | 1462 | Missense Mutation | CGT,TGT | R478C | NP_037511.2 |
| XM_005266075.3 | 1462 | Missense Mutation | CGT,TGT | R551C | XP_005266132.1 |
| XM_006717083.3 | 1462 | UTR 3 | XP_006717146.1 | ||
| XM_011518599.2 | 1462 | Missense Mutation | CGT,TGT | R500C | XP_011516901.1 |
| XM_011518600.1 | 1462 | Missense Mutation | CGT,TGT | R470C | XP_011516902.1 |
| XM_017014651.1 | 1462 | UTR 3 | XP_016870140.1 | ||
| XM_017014652.1 | 1462 | UTR 3 | XP_016870141.1 |