Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001320523.1 | 133 | Missense Mutation | CTG,GTG | L21V | NP_001307452.1 |
NM_004710.4 | 133 | Missense Mutation | CTG,GTG | L21V | NP_004701.1 |
XM_005257792.3 | 133 | Intron | XP_005257849.1 |