| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001291822.1 | 381 | Missense Mutation | ATG,GTG | M47V | NP_001278751.1 |
| NM_001291823.1 | 381 | Missense Mutation | ATG,GTG | M47V | NP_001278752.1 |
| NM_016523.2 | 381 | Missense Mutation | ATG,GTG | M47V | NP_057607.1 |
| XM_017019414.1 | 381 | Missense Mutation | ATG,GTG | M47V | XP_016874903.1 |
| XM_017019415.1 | 381 | Missense Mutation | ATG,GTG | M47V | XP_016874904.1 |