ENST00000236671.7:c.971A>T
MANE Select
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ENSP00000236671.2:p.Glu324Val
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ENST00000367196.4:c.866A>T
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ENSP00000356164.4:p.Glu289Val
|
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ENST00000427721.3:c.396A>T
|
|
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ENST00000429746.2:c.866A>T
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ENSP00000402586.2:p.Glu289Val
|
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ENST00000433655.6:c.*137A>T
|
ENSP00000404902.1:n.*137A>T
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ENST00000438213.6:c.1088A>T
|
ENSP00000415036.2:p.Glu363Val
|
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ENST00000497544.3:n.587A>T
|
|
|
ENST00000636397.1:c.971A>T
|
ENSP00000489910.1:p.Glu324Val
|
|
ENST00000636571.1:c.950A>T
|
ENSP00000490770.1:p.Glu317Val
|
|
ENST00000636615.1:c.971A>T
|
ENSP00000490014.1:p.Glu324Val
|
|
ENST00000636843.1:c.965A>T
|
ENSP00000490897.1:p.Glu322Val
|
|
ENST00000637158.1:n.569A>T
|
|
|
ENST00000637381.2:n.3399A>T
|
|
|
ENST00000637387.1:c.971A>T
|
ENSP00000490598.1:p.Glu324Val
|
|
ENST00000637815.2:c.953A>T
|
ENSP00000490344.1:p.Glu318Val
|
|
ENST00000637915.1:c.971A>T
|
ENSP00000490471.1:p.Glu324Val
|
|
ENST00000637937.1:n.279A>T
|
|
|
ENST00000678991.1:c.*832A>T
|
ENSP00000503019.1:n.*832A>T
|
|
ENST00000236671.6:c.971A>T
|
ENSP00000236671.2:p.Glu324Val
|
|
ENST00000427721.2:c.371A>T
|
ENSP00000415840.2:p.Glu124Val
|
|
ENST00000429746.1:c.302A>T
|
ENSP00000402586.1:p.Glu101Val
|
|
ENST00000433655.5:c.*137A>T
|
ENSP00000404902.1:n.*137A>T
|
|
ENST00000497544.1:n.587A>T
|
|
|
NM_001909.4:c.971A>T
|
NP_001900.1:p.Glu324Val
|
|
NM_001909.5:c.971A>T
MANE Select
|
NP_001900.1:p.Glu324Val
|
|