| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001301163.1 | 1819 | Missense Mutation | CCC,CGC | P427R | NP_001288092.1 |
| NM_032842.3 | 1819 | Missense Mutation | CCC,CGC | P469R | NP_116231.2 |
| XM_005250655.1 | 1819 | Missense Mutation | CCC,CGC | P468R | XP_005250712.1 |
| XM_011516646.2 | 1819 | Missense Mutation | CCC,CGC | P468R | XP_011514948.1 |