Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001272095.1 | 746 | Missense Mutation | CTG,GTG | L21V | NP_001259024.1 |
NM_001272096.1 | 746 | Missense Mutation | CTG,GTG | L97V | NP_001259025.1 |
NM_004604.4 | 746 | Missense Mutation | CTG,GTG | L99V | NP_004595.2 |
XM_005255521.1 | 746 | Missense Mutation | CTG,GTG | L95V | XP_005255578.1 |
XM_011545925.2 | 746 | Intron | XP_011544227.1 |