| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_032445.2 | 3491 | Missense Mutation | CCG,CTG | P974L | NP_115821.2 |
| XM_017022670.1 | 3491 | Missense Mutation | CCG,CTG | P1027L | XP_016878159.1 |
| XM_017022671.1 | 3491 | Missense Mutation | CCG,CTG | P1070L | XP_016878160.1 |
| XM_017022672.1 | 3491 | Missense Mutation | CCG,CTG | P974L | XP_016878161.1 |
| XM_017022673.1 | 3491 | Intron | XP_016878162.1 | ||
| XM_017022674.1 | 3491 | Missense Mutation | CCG,CTG | P784L | XP_016878163.1 |
| XM_017022675.1 | 3491 | Missense Mutation | CCG,CTG | P784L | XP_016878164.1 |