Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001098272.2 | 1628 | Missense Mutation | CCC,CTC | P503L | NP_001091742.1 |
NM_001324219.1 | 1628 | Missense Mutation | CCC,CTC | P503L | NP_001311148.1 |
NM_001324220.1 | 1628 | Missense Mutation | CCC,CTC | P503L | NP_001311149.1 |
NM_001324222.1 | 1628 | Missense Mutation | CCC,CTC | P461L | NP_001311151.1 |
NM_001324223.1 | 1628 | Missense Mutation | CCC,CTC | P461L | NP_001311152.1 |
NM_001324224.1 | 1628 | Missense Mutation | CCC,CTC | P461L | NP_001311153.1 |
NM_002130.7 | 1628 | Missense Mutation | CCC,CTC | P503L | NP_002121.4 |
XM_011514036.2 | 1628 | Missense Mutation | CCC,CTC | P306L | XP_011512338.1 |
XM_017009412.1 | 1628 | Missense Mutation | CCC,CTC | P503L | XP_016864901.1 |