Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001039362.1 | 2312 | UTR 3 | NP_001034451.1 | ||
NM_144583.3 | 2312 | UTR 3 | NP_653184.2 | ||
XM_011510339.2 | 2312 | Intron | XP_011508641.1 | ||
XM_011510340.2 | 2312 | Intron | XP_011508642.1 | ||
XM_011510341.2 | 2312 | Intron | XP_011508643.1 | ||
XM_017003745.1 | 2312 | Intron | XP_016859234.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001282704.1 | 2312 | Missense Mutation | ATG,GTG | M473V | NP_001269633.1 |
NM_001282705.1 | 2312 | Missense Mutation | ATG,GTG | M469V | NP_001269634.1 |
NM_001282706.1 | 2312 | Missense Mutation | ATG,GTG | M426V | NP_001269635.1 |
NM_001282707.1 | 2312 | Missense Mutation | ATG,GTG | M418V | NP_001269636.1 |
NM_005742.3 | 2312 | Missense Mutation | ATG,GTG | M421V | NP_005733.1 |
XM_011510308.1 | 2312 | Silent Mutation | CCA,CCG | P388P | XP_011508610.1 |