| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001122979.2 | 1657 | Intron | NP_001116451.1 | ||
| NM_001170631.1 | 1657 | Missense Mutation | ATG,GTG | M483V | NP_001164102.1 |
| NM_032029.4 | 1657 | Intron | NP_114418.2 | ||
| XM_011510051.2 | 1657 | Missense Mutation | ATG,GTG | M483V | XP_011508353.1 |
| XM_011510052.2 | 1657 | Missense Mutation | ATG,GTG | M471V | XP_011508354.1 |
| XM_017002442.1 | 1657 | Missense Mutation | ATG,GTG | M483V | XP_016857931.1 |