ENST00000682424.1:c.1480G>C
|
ENSP00000507321.1:p.Glu494Gln
|
|
ENST00000299427.12:c.1594G>C
MANE Select
|
ENSP00000299427.6:p.Glu532Gln
|
|
ENST00000524611.2:n.633G>C
|
|
|
ENST00000524924.2:n.714G>C
|
|
|
ENST00000533371.6:c.865G>C
|
ENSP00000437066.1:p.Glu289Gln
|
|
ENST00000642892.1:c.865G>C
|
ENSP00000494165.1:p.Glu289Gln
|
|
ENST00000643342.1:c.667G>C
|
|
|
ENST00000643439.1:c.*1334G>C
|
ENSP00000495849.1:n.*1334G>C
|
|
ENST00000643479.1:n.1780G>C
|
|
|
ENST00000643516.1:c.1103G>C
|
|
|
ENST00000644218.1:c.1405G>C
|
ENSP00000493574.1:p.Glu469Gln
|
|
ENST00000644683.1:c.*1047G>C
|
ENSP00000494085.1:n.*1047G>C
|
|
ENST00000644810.1:c.1315G>C
|
ENSP00000495895.1:p.Glu439Gln
|
|
ENST00000644831.1:n.1770G>C
|
|
|
ENST00000644933.1:c.*460G>C
|
ENSP00000496133.1:n.*460G>C
|
|
ENST00000645285.1:c.*460G>C
|
ENSP00000495058.1:n.*460G>C
|
|
ENST00000645331.1:n.2799G>C
|
|
|
ENST00000645620.1:c.865G>C
|
ENSP00000493657.1:p.Glu289Gln
|
|
ENST00000646691.1:n.1481G>C
|
|
|
ENST00000646777.1:n.1927G>C
|
|
|
ENST00000647016.1:n.2074G>C
|
|
|
ENST00000647152.1:c.865G>C
|
ENSP00000495893.1:p.Glu289Gln
|
|
ENST00000647209.1:c.*1463G>C
|
ENSP00000495558.1:n.*1463G>C
|
|
ENST00000647346.1:n.2614G>C
|
|
|
ENST00000299427.10:c.1594G>C
|
ENSP00000299427.6:p.Glu532Gln
|
|
ENST00000533371.5:c.865G>C
|
ENSP00000437066.1:p.Glu289Gln
|
|
ENST00000611494.4:c.1594G>C
|
ENSP00000484546.1:p.Glu532Gln
|
|
NM_000391.3:c.1594G>C
|
NP_000382.3:p.Glu532Gln
|
|
NM_000391.4:c.1594G>C
MANE Select
|
NP_000382.3:p.Glu532Gln
|
|