Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001099439.1 | 2925 | Silent Mutation | CTG,TTG | L947L | NP_001092909.1 |
NM_173641.2 | 2925 | Intron | NP_775912.2 | ||
XM_017001080.1 | 2925 | Silent Mutation | CTG,TTG | L550L | XP_016856569.1 |
XM_017001081.1 | 2925 | Missense Mutation | CCT,CTT | P552L | XP_016856570.1 |