| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_014037.2 | 1625 | Missense Mutation | CGC,GGC | R459G | NP_054756.2 |
| XM_005258820.2 | 1625 | Missense Mutation | CGC,GGC | R459G | XP_005258877.1 |
| XM_006723168.3 | 1625 | Missense Mutation | CGC,GGC | R459G | XP_006723231.1 |
| XM_011526859.2 | 1625 | Missense Mutation | CGC,GGC | R504G | XP_011525161.2 |
| XM_011526860.2 | 1625 | Missense Mutation | CGC,GGC | R481G | XP_011525162.1 |
| XM_011526861.2 | 1625 | Missense Mutation | CGC,GGC | R312G | XP_011525163.1 |
| XM_017026712.1 | 1625 | Missense Mutation | CGC,GGC | R541G | XP_016882201.1 |