| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001271641.1 | 1066 | Intron | NP_001258570.1 | ||
| NM_014341.2 | 1066 | Intron | NP_055156.1 | ||
| XM_005248978.1 | 1066 | Missense Mutation | CGT,GGT | R411G | XP_005249035.1 |
| XM_005248979.1 | 1066 | Missense Mutation | CGT,GGT | R394G | XP_005249036.1 |
| XM_011514450.1 | 1066 | Missense Mutation | CGT,GGT | R238G | XP_011512752.1 |
| XM_017010642.1 | 1066 | Missense Mutation | CGT,GGT | R255G | XP_016866131.1 |
| XM_017010643.1 | 1066 | Intron | XP_016866132.1 |