Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001311311.1 | 472 | Missense Mutation | CAT,TAT | H68Y | NP_001298240.1 |
NM_024006.5 | 472 | Missense Mutation | CAT,TAT | H68Y | NP_076869.1 |
NM_206824.2 | 472 | Intron | NP_996560.1 |