| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001242826.1 | 962 | Missense Mutation | ATG,ATT | M177I | NP_001229755.1 |
| NM_005785.3 | 962 | Missense Mutation | ATG,ATT | M177I | NP_005776.1 |
| NM_194358.2 | 962 | Missense Mutation | ATG,ATT | M106I | NP_919339.1 |
| NM_194359.2 | 962 | Missense Mutation | ATG,ATT | M177I | NP_919340.1 |
| XM_005268561.4 | 962 | Missense Mutation | ATG,ATT | M106I | XP_005268618.1 |
| XM_011537734.2 | 962 | Missense Mutation | ATG,ATT | M106I | XP_011536036.1 |
| XM_011537735.2 | 962 | Missense Mutation | ATG,ATT | M106I | XP_011536037.1 |