Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_024689.2 | 972 | Intron | NP_078965.2 | ||
NM_176819.3 | 972 | Silent Mutation | CTG,TTG | L366L | NP_789789.2 |
XM_005272670.1 | 972 | Silent Mutation | CTG,TTG | L308L | XP_005272727.1 |
XM_006724559.1 | 972 | Silent Mutation | CTG,TTG | L282L | XP_006724622.1 |