Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001286216.1 | 1513 | Silent Mutation | CTG,TTG | L389L | NP_001273145.1 |
NM_019096.4 | 1513 | Silent Mutation | CTG,TTG | L477L | NP_061969.3 |
XM_017010976.1 | 1513 | Silent Mutation | CTG,TTG | L477L | XP_016866465.1 |