Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004420.2 | 1775 | Missense Mutation | CAC,CGC | H207R | NP_004411.2 |
XM_011519932.2 | 1775 | Missense Mutation | CAC,CGC | H207R | XP_011518234.1 |
XM_011519933.2 | 1775 | Missense Mutation | CAC,CGC | H207R | XP_011518235.1 |