Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001104577.1 | 1468 | Missense Mutation | CCA,CTA | P252L | NP_001098047.1 |
NM_017986.3 | 1468 | Missense Mutation | CCA,CTA | P252L | NP_060456.3 |
XM_011523951.1 | 1468 | Missense Mutation | CCA,CTA | P252L | XP_011522253.1 |