ENST00000461574.2:c.4272G>C
|
ENSP00000417241.2:p.Gln1424His
|
|
ENST00000470026.6:c.4272G>C
|
ENSP00000419274.2:p.Gln1424His
|
|
ENST00000473961.6:c.4146G>C
|
ENSP00000420201.2:p.Gln1382His
|
|
ENST00000476777.6:c.4266G>C
|
ENSP00000417554.2:p.Gln1422His
|
|
ENST00000477152.6:c.4194G>C
|
ENSP00000419988.2:p.Gln1398His
|
|
ENST00000478531.6:c.960G>C
|
ENSP00000420412.2:p.Gln320His
|
|
ENST00000489037.2:c.4194G>C
|
ENSP00000420781.2:p.Gln1398His
|
|
ENST00000493919.6:c.822G>C
|
ENSP00000418819.2:p.Gln274His
|
|
ENST00000494123.6:c.4272G>C
|
ENSP00000419103.2:p.Gln1424His
|
|
ENST00000497488.2:c.3384G>C
|
ENSP00000418986.2:p.Gln1128His
|
|
ENST00000618469.2:c.4272G>C
|
ENSP00000478114.2:p.Gln1424His
|
|
ENST00000634433.2:c.4149G>C
|
ENSP00000489431.2:p.Gln1383His
|
|
ENST00000644379.2:c.4272G>C
|
ENSP00000496570.2:p.Gln1424His
|
|
ENST00000644555.2:c.822G>C
|
ENSP00000494614.2:p.Gln274His
|
|
ENST00000652672.2:c.4131G>C
|
ENSP00000498906.2:p.Gln1377His
|
|
ENST00000484087.6:c.837G>C
|
ENSP00000419481.2:p.Gln279His
|
|
ENST00000700182.1:c.882G>C
|
ENSP00000514849.1:p.Gln294His
|
|
ENST00000357654.9:c.4272G>C
MANE Select
|
ENSP00000350283.3:p.Gln1424His
|
|
ENST00000471181.7:c.4272G>C
|
ENSP00000418960.2:p.Gln1424His
|
|
ENST00000644379.1:c.593G>C
|
|
|
ENST00000352993.7:c.846G>C
|
ENSP00000312236.5:p.Gln282His
|
|
ENST00000357654.7:c.4272G>C
|
ENSP00000350283.3:p.Gln1424His
|
|
ENST00000461221.5:c.*4055G>C
|
ENSP00000418548.1:n.*4055G>C
|
|
ENST00000461574.1:c.566G>C
|
|
|
ENST00000468300.5:c.963G>C
|
ENSP00000417148.1:p.Gln321His
|
|
ENST00000471181.6:c.4272G>C
|
ENSP00000418960.2:p.Gln1424His
|
|
ENST00000478531.5:c.960G>C
|
ENSP00000420412.1:p.Gln320His
|
|
ENST00000484087.5:c.585G>C
|
ENSP00000419481.1:p.Gln195His
|
|
ENST00000487825.5:c.588G>C
|
ENSP00000418212.1:p.Gln196His
|
|
ENST00000491747.6:c.963G>C
|
ENSP00000420705.2:p.Gln321His
|
|
ENST00000493795.5:c.4131G>C
|
ENSP00000418775.1:p.Gln1377His
|
|
ENST00000493919.5:c.822G>C
|
ENSP00000418819.1:p.Gln274His
|
|
ENST00000586385.5:c.5-18538G>C
|
ENSP00000465818.1:n.5-18538G>C
|
|
ENST00000591534.5:c.-43-7968G>C
|
ENSP00000467329.1:n.-43-7968G>C
|
|
ENST00000591849.5:c.-98-32299G>C
|
ENSP00000465347.1:n.-98-32299G>C
|
|
ENST00000621897.1:n.166G>C
|
|
|
NM_007294.3:c.4272G>C , LRG_292t1:c.4272G>C
|
NP_009225.1:p.Gln1424His
|
|
NM_007297.3:c.4131G>C
|
NP_009228.2:p.Gln1377His
|
|
NM_007298.3:c.963G>C
|
NP_009229.2:p.Gln321His
|
|
NM_007299.3:c.963G>C
|
NP_009230.2:p.Gln321His
|
|
NM_007300.3:c.4272G>C
|
NP_009231.2:p.Gln1424His
|
|
NR_027676.1:n.4408G>C
|
|
|
NM_007294.4:c.4272G>C
MANE Select
|
NP_009225.1:p.Gln1424His
|
|
NM_007297.4:c.4131G>C
|
NP_009228.2:p.Gln1377His
|
|
NM_007299.4:c.963G>C
|
NP_009230.2:p.Gln321His
|
|
NM_007300.4:c.4272G>C
|
NP_009231.2:p.Gln1424His
|
|
NR_027676.2:n.4449G>C
|
|
|