Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145293.1 | 1725 | Missense Mutation | AGT,GGT | S581G | NP_001138765.1 |
NM_001145294.1 | 1725 | Missense Mutation | AGT,GGT | S557G | NP_001138766.1 |
NM_001145295.1 | 1725 | Silent Mutation | ACA,ACG | T539T | NP_001138767.1 |
NM_018297.3 | 1725 | Missense Mutation | AGT,GGT | S599G | NP_060767.2 |
XM_005265316.1 | 1725 | Missense Mutation | AGT,GGT | S544G | XP_005265373.1 |
XM_005265317.1 | 1725 | Silent Mutation | ACA,ACG | T484T | XP_005265374.1 |
XM_011533944.1 | 1725 | Missense Mutation | AGT,GGT | S522G | XP_011532246.1 |
XM_011533945.2 | 1725 | Intron | XP_011532247.1 | ||
XM_017006839.1 | 1725 | Intron | XP_016862328.1 |