Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001291494.1 | 3551 | Missense Mutation | CCA,CTA | P996L | NP_001278423.1 |
NM_003638.2 | 3551 | Missense Mutation | CCA,CTA | P1011L | NP_003629.2 |
XM_011519752.2 | 3551 | Intron | XP_011518054.1 |