Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001281303.1 | 1486 | Silent Mutation | TGC,TGT | C450C | NP_001268232.1 |
NM_006415.3 | 1486 | Missense Mutation | GCG,GTG | A461V | NP_006406.1 |
NM_178324.2 | 1486 | Intron | NP_847894.1 | ||
XM_011518138.2 | 1486 | Intron | XP_011516440.1 | ||
XM_011518139.2 | 1486 | Missense Mutation | GCG,GTG | A306V | XP_011516441.1 |
XM_017014200.1 | 1486 | Missense Mutation | GCG,GTG | A339V | XP_016869689.1 |
XM_017014201.1 | 1486 | Missense Mutation | GCG,GTG | A339V | XP_016869690.1 |
XM_017014202.1 | 1486 | Missense Mutation | GCG,GTG | A334V | XP_016869691.1 |