Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001001710.2 | 1799 | Missense Mutation | AGC,GGC | S278G | NP_001001710.1 |
XM_006717108.2 | 1799 | Missense Mutation | AGC,GGC | S262G | XP_006717171.2 |
XM_011518694.1 | 1799 | Missense Mutation | AGC,GGC | S313G | XP_011516996.1 |
XM_011518695.1 | 1799 | Missense Mutation | AGC,GGC | S275G | XP_011516997.1 |
XM_011518696.2 | 1799 | Intron | XP_011516998.1 | ||
XM_011518697.1 | 1799 | UTR 3 | XP_011516999.1 | ||
XM_017014718.1 | 1799 | Missense Mutation | AGC,GGC | S191G | XP_016870207.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006088.5 | 1799 | Intron | NP_006079.1 |