Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_033402.4 | 177 | Missense Mutation | CAC,CAG | H34Q | NP_208325.3 |
XM_005251318.3 | 177 | Missense Mutation | ACA,AGA | T10R | XP_005251375.1 |
XM_005251319.4 | 177 | UTR 5 | XP_005251376.1 | ||
XM_005251320.3 | 177 | UTR 5 | XP_005251377.1 | ||
XM_005251322.3 | 177 | UTR 5 | XP_005251379.1 | ||
XM_017013920.1 | 177 | Missense Mutation | CAC,CAG | H34Q | XP_016869409.1 |
XM_017013921.1 | 177 | Missense Mutation | CAC,CAG | H34Q | XP_016869410.1 |
XM_017013922.1 | 177 | Missense Mutation | CAC,CAG | H34Q | XP_016869411.1 |
XM_017013923.1 | 177 | Missense Mutation | ACA,AGA | T10R | XP_016869412.1 |
XM_017013924.1 | 177 | Missense Mutation | CAC,CAG | H34Q | XP_016869413.1 |
XM_017013925.1 | 177 | Intron | XP_016869414.1 | ||
XM_017013926.1 | 177 | UTR 5 | XP_016869415.1 | ||
XM_017013927.1 | 177 | UTR 5 | XP_016869416.1 | ||
XM_017013928.1 | 177 | Intron | XP_016869417.1 |