| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_018034.2 | 378 | Missense Mutation | ACG,ATG | T101M | NP_060504.1 |
| XM_005248318.3 | 378 | Missense Mutation | ACG,ATG | T100M | XP_005248375.1 |
| XM_011514061.2 | 378 | Intron | XP_011512363.1 | ||
| XM_017009604.1 | 378 | Intron | XP_016865093.1 | ||
| XM_017009605.1 | 378 | Intron | XP_016865094.1 |