ENST00000413384.7:c.207A>T
MANE Select
|
ENSP00000405600.2:p.Glu69Asp
|
|
ENST00000677246.1:c.207A>T
|
ENSP00000504447.1:p.Glu69Asp
|
|
ENST00000310317.9:c.52-248A>T
|
ENSP00000311402.5:n.52-248A>T
|
|
ENST00000392826.6:c.180A>T
|
ENSP00000376571.2:p.Glu60Asp
|
|
ENST00000413384.6:c.207A>T
|
ENSP00000405600.2:p.Glu69Asp
|
|
ENST00000461735.1:c.165A>T
|
ENSP00000419164.1:p.Glu55Asp
|
|
ENST00000463414.5:c.207A>T
|
ENSP00000418584.1:p.Glu69Asp
|
|
ENST00000482950.5:c.207A>T
|
ENSP00000419379.1:p.Glu69Asp
|
|
ENST00000483786.5:c.207A>T
|
ENSP00000417808.1:p.Glu69Asp
|
|
ENST00000485713.5:c.207A>T
|
ENSP00000419412.1:p.Glu69Asp
|
|
ENST00000488420.1:c.207A>T
|
ENSP00000417221.1:p.Glu69Asp
|
|
ENST00000490898.5:c.207A>T
|
ENSP00000418114.1:p.Glu69Asp
|
|
ENST00000494125.1:n.442A>T
|
|
|
NM_001199692.1:c.207A>T
|
NP_001186621.1:p.Glu69Asp
|
|
NM_001199693.1:c.180A>T
|
NP_001186622.1:p.Glu60Asp
|
|
NM_001199694.1:c.165A>T
|
NP_001186623.1:p.Glu55Asp
|
|
NM_003040.3:c.207A>T
|
NP_003031.3:p.Glu69Asp
|
|
XM_006716094.2:c.207A>T
|
XP_006716157.1:p.Glu69Asp
|
|
XM_011516497.1:c.207A>T
|
XP_011514799.1:p.Glu69Asp
|
|
NM_001199692.2:c.207A>T
|
NP_001186621.1:p.Glu69Asp
|
|
NM_001199694.2:c.165A>T
|
NP_001186623.1:p.Glu55Asp
|
|
XM_006716094.3:c.207A>T
|
XP_006716157.1:p.Glu69Asp
|
|
NM_003040.4:c.207A>T
MANE Select
|
NP_003031.3:p.Glu69Asp
|
|
NM_001199692.3:c.207A>T
|
NP_001186621.1:p.Glu69Asp
|
|