Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001823.4 | 1088 | Silent Mutation | CTG,CTT | L312L | NP_001814.2 |
XM_017020951.1 | 1088 | Silent Mutation | CTG,CTT | L336L | XP_016876440.1 |
XM_017020952.1 | 1088 | Intron | XP_016876441.1 |