| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001308229.1 | 366 | Missense Mutation | CGT,TGT | R111C | NP_001295158.1 |
| NM_173657.2 | 366 | Missense Mutation | CGT,TGT | R68C | NP_775928.1 |
| XM_005247379.4 | 366 | Intron | XP_005247436.1 | ||
| XM_011512710.2 | 366 | Missense Mutation | CGT,TGT | R91C | XP_011511012.1 |
| XM_011512711.2 | 366 | Intron | XP_011511013.1 |