| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001098199.1 | 817 | Missense Mutation | CCC,CTC | P198L | NP_001091669.1 |
| NM_001261452.1 | 817 | Missense Mutation | CCC,CTC | P198L | NP_001248381.1 |
| NM_001261453.1 | 817 | Missense Mutation | CCC,CTC | P198L | NP_001248382.1 |
| NM_001261454.1 | 817 | Missense Mutation | CCC,CTC | P198L | NP_001248383.1 |
| NM_001261455.1 | 817 | Missense Mutation | CCC,CTC | P198L | NP_001248384.1 |
| NM_005279.3 | 817 | Missense Mutation | CCC,CTC | P198L | NP_005270.2 |
| XM_005246471.2 | 817 | Missense Mutation | CCC,CTC | P198L | XP_005246528.1 |
| XM_017003832.1 | 817 | Missense Mutation | CCC,CTC | P198L | XP_016859321.1 |