| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000020.2 | 223 | Missense Mutation | CCG,CTG | P26L | NP_000011.2 |
| NM_001077401.1 | 223 | Missense Mutation | CCG,CTG | P26L | NP_001070869.1 |
| XM_005269235.2 | 223 | Missense Mutation | CCG,CTG | P26L | XP_005269292.1 |
| XM_011539008.1 | 223 | Missense Mutation | CCG,CTG | P40L | XP_011537310.1 |