| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001242.4 | 266 | Missense Mutation | AGG,GGG | R13G | NP_001233.1 |
| XM_011521042.2 | 266 | Intron | XP_011519344.1 | ||
| XM_017020232.1 | 266 | Missense Mutation | AGG,GGG | R13G | XP_016875721.1 |
| XM_017020233.1 | 266 | Intron | XP_016875722.1 | ||
| XM_017020234.1 | 266 | Missense Mutation | AGG,GGG | R13G | XP_016875723.1 |