Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001302959.1 | 177 | Intron | NP_001289888.1 | ||
NM_001302960.1 | 177 | Missense Mutation | CAT,CGT | H16R | NP_001289889.1 |
NM_003977.3 | 177 | Missense Mutation | CAT,CGT | H16R | NP_003968.3 |