Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_052935.4 | 866 | Missense Mutation | CAC,CGC | H263R | NP_443167.4 |
XM_006721669.3 | 866 | Missense Mutation | CAC,CGC | H220R | XP_006721732.1 |
XM_006721670.3 | 866 | Missense Mutation | CAC,CGC | H220R | XP_006721733.1 |
XM_011524276.2 | 866 | Missense Mutation | CAC,CGC | H196R | XP_011522578.1 |
XM_011524277.2 | 866 | Missense Mutation | CAC,CGC | H188R | XP_011522579.1 |
XM_017024127.1 | 866 | UTR 3 | XP_016879616.1 |