Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_002291.2 | 5492 | Silent Mutation | GCC,GCT | A1719A | NP_002282.2 |
XM_017012201.1 | 5492 | Silent Mutation | GCC,GCT | A1743A | XP_016867690.1 |
XM_017012202.1 | 5492 | Intron | XP_016867691.1 |