Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001257370.1 | 425 | Missense Mutation | CCC,CTC | P168L | NP_001244299.1 |
XM_017023025.1 | 425 | Missense Mutation | CCC,CTC | P140L | XP_016878514.1 |
XM_017023026.1 | 425 | Missense Mutation | CCC,CTC | P137L | XP_016878515.1 |