| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_017829.5 | 46 | Missense Mutation | ATG,ATT | M1I | NP_060299.4 |
| NM_033070.2 | 46 | Intron | NP_149061.1 | ||
| XM_005261236.3 | 46 | Intron | XP_005261293.1 | ||
| XM_011546126.2 | 46 | Intron | XP_011544428.1 | ||
| XM_011546127.1 | 46 | Intron | XP_011544429.1 | ||
| XM_017028781.1 | 46 | Intron | XP_016884270.1 | ||
| XM_017028782.1 | 46 | Intron | XP_016884271.1 | ||
| XM_017028783.1 | 46 | Intron | XP_016884272.1 | ||
| XM_017028784.1 | 46 | Intron | XP_016884273.1 |