Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003613.3 | 3677 | Missense Mutation | AGT,GGT | S1166G | NP_003604.3 |
XM_017022678.1 | 3677 | Missense Mutation | AGT,GGT | S1193G | XP_016878167.1 |
XM_017022679.1 | 3677 | Missense Mutation | AGT,GGT | S1142G | XP_016878168.1 |