Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001042410.1 | 1619 | Intron | NP_001035869.1 | ||
NM_001282792.1 | 1619 | Intron | NP_001269721.1 | ||
NM_018089.2 | 1619 | Intron | NP_060559.2 | ||
XM_005246663.2 | 1619 | Intron | XP_005246720.1 | ||
XM_011511392.2 | 1619 | Intron | XP_011509694.1 | ||
XM_017004420.1 | 1619 | Intron | XP_016859909.1 | ||
XM_017004421.1 | 1619 | Intron | XP_016859910.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001286423.1 | 1619 | Missense Mutation | CCT,GCT | P611A | NP_001273352.1 |
NM_001286427.1 | 1619 | Missense Mutation | CCT,GCT | P521A | NP_001273356.1 |
NM_024506.4 | 1619 | Missense Mutation | CCT,GCT | P611A | NP_078782.3 |
XM_011511813.2 | 1619 | Missense Mutation | CCT,GCT | P368A | XP_011510115.1 |
XM_017004895.1 | 1619 | Missense Mutation | CCT,GCT | P521A | XP_016860384.1 |