| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001319145.1 | 342 | Missense Mutation | ACG,ATG | T55M | NP_001306074.1 |
| NM_001766.3 | 342 | Missense Mutation | ACG,ATG | T55M | NP_001757.1 |
| XM_005245583.1 | 342 | UTR 5 | XP_005245640.1 | ||
| XM_006711621.1 | 342 | UTR 5 | XP_006711684.1 | ||
| XM_011510125.1 | 342 | Missense Mutation | ACG,ATG | T55M | XP_011508427.1 |
| XM_011510127.1 | 342 | UTR 5 | XP_011508429.1 |