Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001307929.1 | 413 | Intron | NP_001294858.1 | ||
NM_006360.5 | 413 | Silent Mutation | CTG,TTG | L90L | NP_006351.2 |
XM_011519840.2 | 413 | Silent Mutation | CTG,TTG | L27L | XP_011518142.1 |