Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_024798.2 | 562 | Missense Mutation | CCC,CTC | P168L | NP_079074.2 |
XM_005254677.3 | 562 | Intron | XP_005254734.1 | ||
XM_017022581.1 | 562 | Missense Mutation | CCC,CTC | P140L | XP_016878070.1 |