| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001130721.1 | 658 | Missense Mutation | ATG,GTG | M176V | NP_001124193.1 |
| NM_024090.2 | 658 | Missense Mutation | ATG,GTG | M176V | NP_076995.1 |
| XM_011532233.2 | 658 | Missense Mutation | ATG,GTG | M176V | XP_011530535.1 |
| XM_011532234.2 | 658 | Missense Mutation | ATG,GTG | M176V | XP_011530536.1 |
| XM_011532235.2 | 658 | Missense Mutation | ATG,GTG | M92V | XP_011530537.1 |