Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001282444.1 | 1462 | Missense Mutation | CCC,CTC | P446L | NP_001269373.1 |
NM_001282445.1 | 1462 | Missense Mutation | CCC,CTC | P460L | NP_001269374.1 |
NM_006795.3 | 1462 | Missense Mutation | CCC,CTC | P446L | NP_006786.2 |
XM_011544739.1 | 1462 | Missense Mutation | CCC,CTC | P446L | XP_011543041.1 |