| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001101653.1 | 366 | Missense Mutation | CGC,TGC | R80C | NP_001095123.1 |
| NM_001307932.1 | 366 | Missense Mutation | ACG,ATG | T110M | NP_001294861.1 |
| NM_001307937.1 | 366 | Missense Mutation | CGC,TGC | R113C | NP_001294866.1 |
| NM_014186.3 | 366 | Missense Mutation | CGC,TGC | R122C | NP_054905.2 |
| XM_017017625.1 | 366 | Intron | XP_016873114.1 |