| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001097620.1 | 2482 | Silent Mutation | GGC,GGT | G391G | NP_001091089.1 |
| XM_006715653.1 | 2482 | Missense Mutation | CGG,TGG | R411W | XP_006715716.1 |
| XM_006715655.2 | 2482 | Silent Mutation | GGC,GGT | G370G | XP_006715718.1 |
| XM_011515164.1 | 2482 | Missense Mutation | CGG,TGG | R391W | XP_011513466.1 |
| XM_011515165.2 | 2482 | Intron | XP_011513467.1 | ||
| XM_011515166.2 | 2482 | Intron | XP_011513468.1 | ||
| XM_017011815.1 | 2482 | UTR 5 | XP_016867304.1 |