Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001301138.1 | 2547 | Missense Mutation | CAC,CGC | H801R | NP_001288067.1 |
NM_015289.3 | 2547 | Missense Mutation | CAC,CGC | H790R | NP_056104.2 |
XM_011521403.2 | 2547 | Missense Mutation | CAC,CGC | H801R | XP_011519705.1 |
XM_011521404.2 | 2547 | Missense Mutation | CAC,CGC | H790R | XP_011519706.1 |
XM_017022036.1 | 2547 | Missense Mutation | CAC,CGC | H801R | XP_016877525.1 |
XM_017022037.1 | 2547 | Missense Mutation | CAC,CGC | H790R | XP_016877526.1 |
XM_017022038.1 | 2547 | Missense Mutation | CAC,CGC | H666R | XP_016877527.1 |
XM_017022039.1 | 2547 | Missense Mutation | CAC,CGC | H433R | XP_016877528.1 |