ENST00000356126.8:c.342A>G
MANE Select
|
ENSP00000348442.3:p.Glu114=
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|
ENST00000356126.7:c.342A>G
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ENSP00000348442.3:p.Glu114=
|
|
ENST00000357146.4:c.282A>G
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ENSP00000349667.4:p.Glu94=
|
|
ENST00000581618.1:n.579A>G
|
|
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ENST00000584008.5:c.*497A>G
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ENSP00000462525.1:n.*497A>G
|
|
ENST00000584289.5:n.391A>G
|
|
|
NM_001316341.1:c.165A>G
|
NP_001303270.1:p.Glu55=
|
|
NM_002816.3:c.342A>G
|
NP_002807.1:p.Glu114=
|
|
NM_002816.4:c.342A>G
|
NP_002807.1:p.Glu114=
|
|
NM_174871.2:c.282A>G
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NP_777360.1:p.Glu94=
|
|
NM_174871.3:c.282A>G
|
NP_777360.1:p.Glu94=
|
|
XM_011525048.1:c.165A>G
|
XP_011523350.1:p.Glu55=
|
|
XM_011525049.1:c.165A>G
|
XP_011523351.1:p.Glu55=
|
|
XM_011525050.1:c.342A>G
|
XP_011523352.1:p.Glu114=
|
|
XM_024450842.1:c.429A>G
|
XP_024306610.1:p.Glu143=
|
|
XM_024450843.1:c.165A>G
|
XP_024306611.1:p.Glu55=
|
|
XR_001752571.2:n.421A>G
|
|
|
NM_002816.5:c.342A>G
MANE Select
|
NP_002807.1:p.Glu114=
|
|
NM_001316341.2:c.165A>G
|
NP_001303270.1:p.Glu55=
|
|
NM_174871.4:c.282A>G
|
NP_777360.1:p.Glu94=
|
|