| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_002977.3 | 5979 | Missense Mutation | CGT,TGT | R1891C | NP_002968.1 |
| XM_005246757.2 | 5979 | Missense Mutation | CGT,TGT | R1902C | XP_005246814.1 |
| XM_011511616.2 | 5979 | Missense Mutation | CGT,TGT | R1902C | XP_011509918.1 |
| XM_011511617.2 | 5979 | Missense Mutation | CGT,TGT | R1902C | XP_011509919.1 |
| XM_011511618.2 | 5979 | Missense Mutation | CGT,TGT | R1891C | XP_011509920.1 |
| XM_011511619.2 | 5979 | Intron | XP_011509921.1 | ||
| XM_017004668.1 | 5979 | Missense Mutation | CGT,TGT | R1773C | XP_016860157.1 |
| XM_017004669.1 | 5979 | Missense Mutation | CGT,TGT | R1654C | XP_016860158.1 |