| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001168316.1 | 1538 | Missense Mutation | ACG,ATG | T435M | NP_001161788.1 |
| NM_174914.3 | 1538 | Missense Mutation | ACG,ATG | T469M | NP_777574.2 |
| XM_011513988.2 | 1538 | Missense Mutation | ACG,ATG | T496M | XP_011512290.1 |
| XM_017009150.1 | 1538 | Missense Mutation | ACG,ATG | T431M | XP_016864639.1 |