| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_152527.4 | 1715 | Missense Mutation | ACG,ATG | T467M | NP_689740.2 |
| XM_005246353.3 | 1715 | Missense Mutation | ACG,ATG | T419M | XP_005246410.1 |
| XM_011510751.2 | 1715 | Missense Mutation | ACG,ATG | T467M | XP_011509053.1 |
| XM_011510752.1 | 1715 | Intron | XP_011509054.1 | ||
| XM_017003480.1 | 1715 | Missense Mutation | ACG,ATG | T467M | XP_016858969.1 |