| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286506.1 | 1087 | Missense Mutation | CTC,TTC | L269F | NP_001273435.1 |
| NM_080860.3 | 1087 | Missense Mutation | CTC,TTC | L307F | NP_543136.1 |
| XM_005261208.2 | 1087 | Missense Mutation | CTC,TTC | L238F | XP_005261265.1 |
| XM_011529786.1 | 1087 | Missense Mutation | CTC,TTC | L283F | XP_011528088.1 |