| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_006076.4 | 366 | Missense Mutation | CGT,TGT | R82C | NP_006067.3 |
| XM_005250306.2 | 366 | Missense Mutation | CGT,TGT | R82C | XP_005250363.1 |
| XM_017012112.1 | 366 | UTR 5 | XP_016867601.1 | ||
| XM_017012113.1 | 366 | Missense Mutation | CGT,TGT | R82C | XP_016867602.1 |
| XM_017012114.1 | 366 | UTR 5 | XP_016867603.1 |