Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_030661.4 | 916 | Intron | NP_109377.1 | ||
NM_153631.2 | 916 | Intron | NP_705895.1 | ||
XM_005249730.2 | 916 | Intron | XP_005249787.1 | ||
XM_005249731.2 | 916 | Intron | XP_005249788.1 | ||
XM_005249732.3 | 916 | Intron | XP_005249789.1 | ||
XM_006715715.2 | 916 | Intron | XP_006715778.1 | ||
XM_011515343.2 | 916 | Intron | XP_011513645.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_002141.4 | 916 | Missense Mutation | TCT,TGT | S290C | NP_002132.3 |