| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001040160.2 | 566 | Missense Mutation | AAG,AGG | K133R | NP_001035250.1 |
| NM_001040161.2 | 566 | Intron | NP_001035251.1 | ||
| NM_001040162.2 | 566 | Missense Mutation | AGG,GGG | R79G | NP_001035252.1 |
| NM_001040165.2 | 566 | Intron | NP_001035255.1 | ||
| NM_001288710.1 | 566 | Intron | NP_001275639.1 | ||
| NM_032366.4 | 566 | Missense Mutation | AAG,AGG | K133R | NP_115742.3 |
| XM_011522713.2 | 566 | Silent Mutation | CAA,CAG | Q164Q | XP_011521015.1 |
| XM_011522714.2 | 566 | Silent Mutation | CAA,CAG | Q164Q | XP_011521016.1 |