Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001001694.2 | 2462 | Missense Mutation | CCT,CTT | P333L | NP_001001694.2 |
XM_011530689.2 | 2462 | Missense Mutation | CCT,CTT | P405L | XP_011528991.1 |
XM_017028798.1 | 2462 | Silent Mutation | GCC,GCT | A427A | XP_016884287.1 |