| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_017770.3 | 958 | Missense Mutation | ACG,ATG | T266M | NP_060240.3 |
| XM_011514716.2 | 958 | Missense Mutation | ACG,ATG | T296M | XP_011513018.1 |
| XM_011514717.2 | 958 | Missense Mutation | ACG,ATG | T267M | XP_011513019.1 |
| XM_017010985.1 | 958 | Intron | XP_016866474.1 |