Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001205262.2 | 2602 | Intron | NP_001192191.1 | ||
NM_001205263.1 | 2602 | Missense Mutation | CAT,CGT | H640R | NP_001192192.1 |
NM_012415.3 | 2602 | Missense Mutation | CAT,CGT | H824R | NP_036547.1 |