Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_199287.2 | 497 | Missense Mutation | CTG,GTG | L187V | NP_954981.1 |
XM_011524738.2 | 497 | Missense Mutation | CTG,GTG | L59V | XP_011523040.1 |
XM_017024573.1 | 497 | Intron | XP_016880062.1 |