| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_014464.3 | 429 | Missense Mutation | CGT,TGT | R95C | NP_055279.3 |
| XM_006715062.2 | 429 | Missense Mutation | CGT,TGT | R77C | XP_006715125.1 |
| XM_011514497.2 | 429 | Missense Mutation | CGT,TGT | R95C | XP_011512799.1 |
| XM_017010745.1 | 429 | Missense Mutation | CGT,TGT | R95C | XP_016866234.1 |
| XM_017010746.1 | 429 | Intron | XP_016866235.1 | ||
| XM_017010747.1 | 429 | Intron | XP_016866236.1 | ||
| XM_017010748.1 | 429 | Intron | XP_016866237.1 |