Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001100159.2 | 148 | Missense Mutation | CAC,CGC | H28R | NP_001093629.1 |
NM_001267865.1 | 148 | UTR 5 | NP_001254794.1 | ||
NM_001267866.1 | 148 | UTR 5 | NP_001254795.1 | ||
XM_006715649.3 | 148 | Missense Mutation | CAC,CGC | H28R | XP_006715712.1 |
XM_006715650.2 | 148 | UTR 5 | XP_006715713.1 | ||
XM_011515121.1 | 148 | Missense Mutation | CAC,CGC | H28R | XP_011513423.1 |
XM_011515122.2 | 148 | Missense Mutation | CAC,CGC | H28R | XP_011513424.1 |
XM_011515123.2 | 148 | Missense Mutation | CAC,CGC | H28R | XP_011513425.1 |