Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_203365.3 | 3521 | Intron | NP_976241.1 | ||
NM_213589.2 | 3521 | Missense Mutation | GCT,GTT | A1147V | NP_998754.1 |
XM_005246777.3 | 3521 | Missense Mutation | GCT,GTT | A1199V | XP_005246834.1 |
XM_005246779.4 | 3521 | Missense Mutation | GCT,GTT | A1199V | XP_005246836.1 |
XM_006712695.3 | 3521 | Missense Mutation | GCT,GTT | A1199V | XP_006712758.1 |
XM_011511646.2 | 3521 | Missense Mutation | GCT,GTT | A1199V | XP_011509948.1 |
XM_011511647.1 | 3521 | Missense Mutation | GCT,GTT | A1174V | XP_011509949.1 |
XM_011511648.1 | 3521 | Missense Mutation | GCT,GTT | A1172V | XP_011509950.1 |
XM_011511649.2 | 3521 | Intron | XP_011509951.1 |