| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_145290.3 | 3857 | Missense Mutation | ACG,AGG | T1196R | NP_660333.2 |
| XM_005248137.4 | 3857 | Intron | XP_005248194.1 | ||
| XM_011513811.2 | 3857 | Missense Mutation | ACG,AGG | T970R | XP_011512113.1 |
| XM_017007834.1 | 3857 | Missense Mutation | ACG,AGG | T999R | XP_016863323.1 |