Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_014008.4 | 1377 | Intron | NP_054727.1 | ||
XM_005272599.3 | 1377 | Intron | XP_005272656.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001114377.1 | 1377 | Missense Mutation | CGG,TGG | R362W | NP_001107849.1 |
NM_014009.3 | 1377 | Missense Mutation | CGG,TGG | R397W | NP_054728.2 |
XM_006724533.2 | 1377 | Missense Mutation | CGG,TGG | R420W | XP_006724596.2 |
XM_011543916.2 | 1377 | Missense Mutation | CGG,TGG | R530W | XP_011542218.1 |
XM_017029565.1 | 1377 | Missense Mutation | CGG,TGG | R482W | XP_016885054.1 |
XM_017029566.1 | 1377 | Missense Mutation | CGG,TGG | R470W | XP_016885055.1 |
XM_017029567.1 | 1377 | Missense Mutation | CGG,TGG | R439W | XP_016885056.1 |