Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_002657.3 | 1388 | Intron | NP_002648.1 | ||
XM_005260436.3 | 1388 | Missense Mutation | CAC,CGC | H109R | XP_005260493.1 |
XM_011528863.2 | 1388 | Missense Mutation | CAC,CGC | H109R | XP_011527165.1 |
XM_011528864.2 | 1388 | Missense Mutation | CAC,CGC | H109R | XP_011527166.1 |