Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004421.2 | 1669 | Missense Mutation | CCC,CTC | P506L | NP_004412.2 |
XM_005244731.3 | 1669 | Missense Mutation | CCC,CTC | P531L | XP_005244788.1 |
XM_005244732.3 | 1669 | Missense Mutation | CCC,CTC | P531L | XP_005244789.1 |
XM_005244733.3 | 1669 | Missense Mutation | CCC,CTC | P506L | XP_005244790.1 |