| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001304492.1 | 2216 | Intron | NP_001291421.1 | ||
| NM_001304493.1 | 2216 | Missense Mutation | CGG,TGG | R407W | NP_001291422.1 |
| NM_001304494.1 | 2216 | Intron | NP_001291423.1 | ||
| NM_145911.2 | 2216 | Missense Mutation | CGG,TGG | R465W | NP_666016.1 |