Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001278505.1 | 243 | Intron | NP_001265434.1 | ||
NM_001322249.1 | 243 | Missense Mutation | CAT,CGT | H59R | NP_001309178.1 |
NM_174931.3 | 243 | Missense Mutation | CAT,CGT | H59R | NP_777591.3 |
XM_017003748.1 | 243 | Intron | XP_016859237.1 |