| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001202475.1 | 2385 | Missense Mutation | CAG,CGG | Q426R | NP_001189404.1 |
| NM_001202481.1 | 2385 | Missense Mutation | CAG,CGG | Q385R | NP_001189410.1 |
| NM_001202482.1 | 2385 | Missense Mutation | CAG,CGG | Q398R | NP_001189411.1 |
| NM_001202483.1 | 2385 | UTR 3 | NP_001189412.1 | ||
| NM_001883.4 | 2385 | Missense Mutation | CAG,CGG | Q399R | NP_001874.2 |
| XM_011515127.2 | 2385 | Silent Mutation | ACA,ACG | T469T | XP_011513429.1 |
| XM_011515128.2 | 2385 | Intron | XP_011513430.1 | ||
| XM_011515129.2 | 2385 | Intron | XP_011513431.1 | ||
| XM_017011751.1 | 2385 | Silent Mutation | ACA,ACG | T468T | XP_016867240.1 |
| XM_017011752.1 | 2385 | Missense Mutation | CAG,CGG | Q385R | XP_016867241.1 |