| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000305.2 | 817 | Missense Mutation | CCT,CTT | P274L | NP_000296.2 |
| NM_001018161.1 | 817 | Missense Mutation | CCT,CTT | P262L | NP_001018171.1 |
| XM_005250453.1 | 817 | Missense Mutation | CCT,CTT | P206L | XP_005250510.1 |
| XM_017012357.1 | 817 | Missense Mutation | CCT,CTT | P204L | XP_016867846.1 |
| XM_017012358.1 | 817 | Missense Mutation | CCT,CTT | P188L | XP_016867847.1 |