Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001002838.3 | 5577 | Missense Mutation | GCT,GGT | A1656G | NP_001002838.1 |
NM_020922.4 | 5577 | Missense Mutation | GCT,GGT | A1713G | NP_065973.2 |
XM_006724593.3 | 5577 | Missense Mutation | GCT,GGT | A1656G | XP_006724656.1 |
XM_011530802.2 | 5577 | Missense Mutation | GCT,GGT | A1666G | XP_011529104.1 |
XM_017029741.1 | 5577 | Missense Mutation | GCT,GGT | A1713G | XP_016885230.1 |
XM_017029742.1 | 5577 | Missense Mutation | GCT,GGT | A1713G | XP_016885231.1 |
XM_017029743.1 | 5577 | Missense Mutation | GCT,GGT | A1713G | XP_016885232.1 |
XM_017029744.1 | 5577 | Missense Mutation | GCT,GGT | A1713G | XP_016885233.1 |
XM_017029745.1 | 5577 | Missense Mutation | GCT,GGT | A1703G | XP_016885234.1 |