| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_024541.2 | 2150 | Missense Mutation | CAG,CGG | Q668R | NP_078817.2 |
| XM_006717969.1 | 2150 | Missense Mutation | CAG,CGG | Q598R | XP_006718032.1 |
| XM_011540151.2 | 2150 | Missense Mutation | CAG,CGG | Q668R | XP_011538453.1 |
| XM_011540152.2 | 2150 | Missense Mutation | CAG,CGG | Q646R | XP_011538454.1 |
| XM_011540153.2 | 2150 | Missense Mutation | CAG,CGG | Q634R | XP_011538455.1 |
| XM_011540154.2 | 2150 | Missense Mutation | CAG,CGG | Q612R | XP_011538456.1 |
| XM_011540156.2 | 2150 | Missense Mutation | CAG,CGG | Q494R | XP_011538458.1 |
| XM_011540157.2 | 2150 | Missense Mutation | CAG,CGG | Q617R | XP_011538459.1 |
| XM_017016635.1 | 2150 | Intron | XP_016872124.1 | ||
| XM_017016636.1 | 2150 | Intron | XP_016872125.1 |