| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001040167.1 | 36 | Missense Mutation | CGG,GGG | R7G | NP_001035257.1 |
| NM_001040168.1 | 36 | Missense Mutation | CGG,GGG | R7G | NP_001035258.1 |
| NM_001166355.1 | 36 | Intron | NP_001159827.1 | ||
| NM_002304.2 | 36 | Intron | NP_002295.1 |