| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001317837.1 | 808 | Missense Mutation | CGG,TGG | R91W | NP_001304766.1 |
| NM_001317838.1 | 808 | Missense Mutation | CGG,TGG | R91W | NP_001304767.1 |
| NM_001317839.1 | 808 | Missense Mutation | CGG,TGG | R91W | NP_001304768.1 |
| NM_001317841.1 | 808 | Missense Mutation | CGG,TGG | R65W | NP_001304770.1 |
| NM_001317842.1 | 808 | Missense Mutation | CGG,TGG | R65W | NP_001304771.1 |
| NM_152399.3 | 808 | Missense Mutation | CGG,TGG | R91W | NP_689612.3 |
| XM_005262737.2 | 808 | Missense Mutation | CGG,TGG | R91W | XP_005262794.1 |
| XM_017007725.1 | 808 | Missense Mutation | CGG,TGG | R91W | XP_016863214.1 |
| XM_017007726.1 | 808 | Missense Mutation | CGG,TGG | R65W | XP_016863215.1 |