Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_138462.2 | 660 | Silent Mutation | GTG,GTT | V146V | NP_612471.1 |
XM_005266052.4 | 660 | Silent Mutation | GTG,GTT | V207V | XP_005266109.1 |
XM_017014255.1 | 660 | Intron | XP_016869744.1 |