| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001102575.1 | 1113 | Missense Mutation | CCG,CTG | P308L | NP_001096045.1 |
| NM_001145427.1 | 1113 | Missense Mutation | CCG,CTG | P308L | NP_001138899.1 |
| NM_052870.2 | 1113 | Missense Mutation | CCG,CTG | P308L | NP_443102.2 |
| XM_017008997.1 | 1113 | Missense Mutation | CCG,CTG | P308L | XP_016864486.1 |