ENST00000253408.11:c.978G>T
|
ENSP00000253408.5:p.Glu326Asp
|
|
ENST00000435360.8:c.978G>T
|
ENSP00000403962.1:p.Glu326Asp
|
|
ENST00000253408.10:c.978G>T
|
ENSP00000253408.5:p.Glu326Asp
|
|
ENST00000435360.7:c.978G>T
|
ENSP00000403962.1:p.Glu326Asp
|
|
ENST00000585543.6:n.131G>T
|
|
|
ENST00000586127.6:n.1507G>T
|
|
|
ENST00000586793.6:c.907-64G>T
|
ENSP00000468500.2:n.907-64G>T
|
|
ENST00000587997.6:n.454G>T
|
|
|
ENST00000588735.3:c.978G>T
MANE Select
|
ENSP00000466598.2:p.Glu326Asp
|
|
ENST00000591327.2:n.2132G>T
|
|
|
ENST00000592320.6:c.619-64G>T
|
ENSP00000465320.1:n.619-64G>T
|
|
ENST00000638281.1:c.978G>T
|
ENSP00000491088.1:p.Glu326Asp
|
|
ENST00000638618.1:c.633G>T
|
ENSP00000492832.1:p.Glu211Asp
|
|
ENST00000639277.1:c.978G>T
|
ENSP00000492432.1:p.Glu326Asp
|
|
ENST00000640552.1:n.992G>T
|
|
|
ENST00000253408.9:c.978G>T
|
ENSP00000253408.4:p.Glu326Asp
|
|
ENST00000376990.8:c.*377G>T
|
ENSP00000366189.4:n.*377G>T
|
|
ENST00000435360.6:c.978G>T
|
ENSP00000403962.1:p.Glu326Asp
|
|
ENST00000585543.5:n.131G>T
|
|
|
ENST00000586793.5:c.978G>T
|
ENSP00000468500.1:p.Glu326Asp
|
|
ENST00000587997.5:c.454G>T
|
|
|
ENST00000588640.5:n.358G>T
|
|
|
ENST00000588735.1:c.83-3269G>T
|
ENSP00000466598.1:n.83-3269G>T
|
|
ENST00000592320.5:c.619-64G>T
|
ENSP00000465320.1:n.619-64G>T
|
|
NM_001131019.2:c.978G>T
|
NP_001124491.1:p.Glu326Asp
|
|
NM_001242376.1:c.978G>T
|
NP_001229305.1:p.Glu326Asp
|
|
NM_002055.4:c.978G>T
|
NP_002046.1:p.Glu326Asp
|
|
NM_001363846.1:c.978G>T
|
NP_001350775.1:p.Glu326Asp
|
|
XM_024450690.1:c.1182G>T
|
XP_024306458.1:p.Glu394Asp
|
|
XM_024450691.1:c.1182G>T
|
XP_024306459.1:p.Glu394Asp
|
|
XM_024450692.1:c.1182G>T
|
XP_024306460.1:p.Glu394Asp
|
|
XM_024450693.1:c.1182G>T
|
XP_024306461.1:p.Glu394Asp
|
|
NM_002055.5:c.978G>T
MANE Select
|
NP_002046.1:p.Glu326Asp
|
|
NM_001131019.3:c.978G>T
|
NP_001124491.1:p.Glu326Asp
|
|
NM_001242376.2:c.978G>T
|
NP_001229305.1:p.Glu326Asp
|
|
NM_001242376.3:c.978G>T
|
NP_001229305.1:p.Glu326Asp
|
|
NM_001363846.2:c.978G>T
|
NP_001350775.1:p.Glu326Asp
|
|