Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_018897.2 | 6274 | Missense Mutation | CAC,CGC | H3926R | NP_061720.2 |
XM_011511487.2 | 6274 | Missense Mutation | CAC,CGC | H3926R | XP_011509789.1 |
XM_011511488.2 | 6274 | Missense Mutation | CAC,CGC | H3886R | XP_011509790.1 |
XM_011511489.2 | 6274 | Missense Mutation | CAC,CGC | H3880R | XP_011509791.1 |
XM_011511490.2 | 6274 | Missense Mutation | CAC,CGC | H3851R | XP_011509792.1 |
XM_011511491.2 | 6274 | Intron | XP_011509793.1 | ||
XM_011511492.2 | 6274 | Intron | XP_011509794.1 | ||
XM_011511493.2 | 6274 | Intron | XP_011509795.1 | ||
XM_011511494.2 | 6274 | Intron | XP_011509796.1 | ||
XM_011511495.2 | 6274 | Intron | XP_011509797.1 | ||
XM_011511497.2 | 6274 | Missense Mutation | CAC,CGC | H2050R | XP_011509799.1 |
XM_017004504.1 | 6274 | Missense Mutation | CAC,CGC | H3835R | XP_016859993.1 |