| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001265597.2 | 425 | Missense Mutation | ACG,ATG | T82M | NP_001252526.1 |
| NM_001265598.2 | 425 | Missense Mutation | ACG,ATG | T69M | NP_001252527.1 |
| NM_001265599.2 | 425 | Missense Mutation | ACG,ATG | T8M | NP_001252528.1 |
| NM_001265600.2 | 425 | Missense Mutation | ACG,ATG | T8M | NP_001252529.1 |
| NM_001322306.1 | 425 | Intron | NP_001309235.1 | ||
| NM_006385.4 | 425 | Missense Mutation | ACG,ATG | T82M | NP_006376.2 |
| NM_198855.3 | 425 | Missense Mutation | ACG,ATG | T69M | NP_942152.1 |