Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001167985.1 | 734 | Intron | NP_001161457.1 | ||
NM_001167986.1 | 734 | Intron | NP_001161458.1 | ||
NM_001167987.1 | 734 | Intron | NP_001161459.1 | ||
NM_213726.2 | 734 | Intron | NP_998891.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006612.5 | 734 | Missense Mutation | CAC,CGC | H129R | NP_006603.2 |
XM_005256424.2 | 734 | Missense Mutation | CAC,CGC | H129R | XP_005256481.1 |