Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_033342.3 | 1201 | Intron | NP_203128.1 | ||
NM_203293.2 | 1201 | Missense Mutation | CAC,CCC | H376P | NP_976038.1 |
NM_203294.1 | 1201 | Missense Mutation | CAC,CCC | H168P | NP_976039.1 |
NM_203295.1 | 1201 | Missense Mutation | CAC,CCC | H168P | NP_976040.1 |
NM_203296.1 | 1201 | Missense Mutation | CAC,CCC | H168P | NP_976041.1 |
NM_203297.1 | 1201 | Missense Mutation | CAC,CCC | H194P | NP_976042.1 |
XM_017009903.1 | 1201 | Missense Mutation | CAC,CCC | H168P | XP_016865392.1 |
XM_017009904.1 | 1201 | Intron | XP_016865393.1 |