Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001291088.1 | 8848 | Missense Mutation | CCC,CTC | P2865L | NP_001278017.1 |
NM_031951.4 | 8848 | Missense Mutation | CCC,CTC | P2826L | NP_114157.4 |
XM_011527360.2 | 8848 | Missense Mutation | CCC,CTC | P2865L | XP_011525662.1 |