Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001080444.1 | 1113 | Intron | NP_001073913.1 | ||
XM_011529472.1 | 1113 | Missense Mutation | CGT,TGT | R3C | XP_011527774.1 |
XM_011529473.1 | 1113 | Missense Mutation | CGT,TGT | R3C | XP_011527775.1 |
XM_017028279.1 | 1113 | Missense Mutation | CGT,TGT | R3C | XP_016883768.1 |
XM_017028280.1 | 1113 | Missense Mutation | CGT,TGT | R3C | XP_016883769.1 |