Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_015527.3 | 1526 | Missense Mutation | CCG,CTG | P503L | NP_056342.3 |
XM_011545789.1 | 1526 | Missense Mutation | CCG,CTG | P398L | XP_011544091.1 |
XM_011545790.2 | 1526 | Intron | XP_011544092.1 |