Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_018467.3 | 173 | Missense Mutation | GCC,GTC | A38V | NP_060937.1 |
XM_017026975.1 | 173 | Missense Mutation | GCC,GTC | A38V | XP_016882464.1 |
XM_017026976.1 | 173 | Intron | XP_016882465.1 |