| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001317964.1 | 3667 | Missense Mutation | ATG,GTG | M1106V | NP_001304893.1 |
| NM_001317965.1 | 3667 | Missense Mutation | ATG,GTG | M1098V | NP_001304894.1 |
| NM_016460.3 | 3667 | Missense Mutation | ATG,GTG | M1125V | NP_057544.2 |
| NM_020117.10 | 3667 | Missense Mutation | ATG,GTG | M1152V | NP_064502.9 |
| XM_011537656.2 | 3667 | Missense Mutation | ATG,GTG | M1098V | XP_011535958.1 |