| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000162.3 | 1759 | Missense Mutation | CCG,CTG | P430L | NP_000153.1 |
| NM_033507.1 | 1759 | Missense Mutation | CCG,CTG | P431L | NP_277042.1 |
| NM_033508.1 | 1759 | Missense Mutation | CCG,CTG | P429L | NP_277043.1 |
| XM_017011966.1 | 1759 | Missense Mutation | CCG,CTG | P430L | XP_016867455.1 |