Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_173546.2 | 1017 | Missense Mutation | CAC,CGC | H106R | NP_775817.1 |
XM_005264938.2 | 1017 | Missense Mutation | CAC,CGC | H106R | XP_005264995.1 |
XM_005264940.4 | 1017 | Intron | XP_005264997.1 | ||
XM_006713015.2 | 1017 | Missense Mutation | CAC,CGC | H106R | XP_006713078.1 |
XM_006713016.2 | 1017 | Missense Mutation | CAC,CGC | H106R | XP_006713079.1 |