| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000958.2 | 1058 | Missense Mutation | ATG,CTG | M156L | NP_000949.1 |
| XM_017009656.1 | 1058 | Missense Mutation | ATG,CTG | M156L | XP_016865145.1 |
| XM_017009657.1 | 1058 | Missense Mutation | ATG,CTG | M156L | XP_016865146.1 |
| XM_017009658.1 | 1058 | Missense Mutation | ATG,CTG | M156L | XP_016865147.1 |
| XM_017009659.1 | 1058 | Missense Mutation | ATG,CTG | M156L | XP_016865148.1 |