| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001145144.1 | 1296 | Missense Mutation | ACG,ATG | T313M | NP_001138616.1 |
| NM_001145145.1 | 1296 | Missense Mutation | ACG,ATG | T339M | NP_001138617.1 |
| NM_005628.2 | 1296 | Missense Mutation | ACG,ATG | T541M | NP_005619.1 |
| XM_005259167.4 | 1296 | Intron | XP_005259224.1 |