Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_018158.2 | 573 | Silent Mutation | CCC,CCT | P97P | NP_060628.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001282729.1 | 573 | Intron | NP_001269658.1 | ||
NM_001282730.1 | 573 | Intron | NP_001269659.1 | ||
NM_001282731.1 | 573 | Intron | NP_001269660.1 | ||
NM_001282732.1 | 573 | Intron | NP_001269661.1 | ||
NM_014860.2 | 573 | Intron | NP_055675.1 | ||
XM_005264672.4 | 573 | Intron | XP_005264729.1 |