ENST00000570382.2:c.672G>T
|
ENSP00000466346.2:p.Glu224Asp
|
|
ENST00000571691.6:c.600G>T
|
ENSP00000461407.2:p.Glu200Asp
|
|
ENST00000571721.6:c.672G>T
|
ENSP00000460660.2:p.Glu224Asp
|
|
ENST00000572105.7:c.*116G>T
|
ENSP00000462823.1:n.*116G>T
|
|
ENST00000573283.7:c.672G>T
MANE Select
|
ENSP00000458435.1:p.Glu224Asp
|
|
ENST00000574671.6:n.1072G>T
|
|
|
ENST00000575659.6:c.672G>T
|
ENSP00000459119.2:p.Glu224Asp
|
|
ENST00000575994.6:c.672G>T
|
ENSP00000460464.2:p.Glu224Asp
|
|
ENST00000576214.3:n.973G>T
|
|
|
ENST00000576544.6:c.672G>T
|
ENSP00000461672.1:p.Glu224Asp
|
|
ENST00000615544.5:c.672G>T
|
ENSP00000477968.1:p.Glu224Asp
|
|
ENST00000644774.2:c.645G>T
|
ENSP00000493648.2:p.Glu215Asp
|
|
ENST00000679410.1:n.796G>T
|
|
|
ENST00000679480.1:c.672G>T
|
ENSP00000506201.1:p.Glu224Asp
|
|
ENST00000679535.1:n.973G>T
|
|
|
ENST00000679778.1:c.672G>T
|
ENSP00000505235.1:p.Glu224Asp
|
|
ENST00000680227.1:c.672G>T
|
ENSP00000506253.1:p.Glu224Asp
|
|
ENST00000680727.1:c.672G>T
|
ENSP00000505193.1:p.Glu224Asp
|
|
ENST00000681052.1:c.672G>T
|
ENSP00000505060.1:p.Glu224Asp
|
|
ENST00000681092.1:c.*476G>T
|
ENSP00000506720.1:n.*476G>T
|
|
ENST00000681842.1:c.672G>T
|
ENSP00000506126.1:p.Glu224Asp
|
|
ENST00000331925.6:c.672G>T
|
ENSP00000331514.2:p.Glu224Asp
|
|
ENST00000571691.5:c.645G>T
|
ENSP00000461407.1:p.Glu215Asp
|
|
ENST00000572105.6:c.*116G>T
|
ENSP00000462823.1:n.*116G>T
|
|
ENST00000573283.5:c.672G>T
|
ENSP00000458435.1:p.Glu224Asp
|
|
ENST00000574671.5:n.531G>T
|
|
|
ENST00000575087.5:c.672G>T
|
ENSP00000459124.1:p.Glu224Asp
|
|
ENST00000575842.5:c.672G>T
|
ENSP00000458162.1:p.Glu224Asp
|
|
ENST00000576209.5:n.557G>T
|
|
|
ENST00000576214.2:n.870G>T
|
|
|
ENST00000576544.5:c.672G>T
|
ENSP00000461672.1:p.Glu224Asp
|
|
ENST00000576917.5:n.725G>T
|
|
|
ENST00000615544.4:c.672G>T
|
ENSP00000477968.1:p.Glu224Asp
|
|
NM_001199954.1:c.672G>T
|
NP_001186883.1:p.Glu224Asp
|
|
NM_001614.3:c.672G>T
|
NP_001605.1:p.Glu224Asp
|
|
NR_037688.1:n.811G>T
|
|
|
NM_001199954.2:c.672G>T
|
NP_001186883.1:p.Glu224Asp
|
|
NM_001614.4:c.672G>T
|
NP_001605.1:p.Glu224Asp
|
|
NR_037688.2:n.744G>T
|
|
|
NM_001614.5:c.672G>T
MANE Select
|
NP_001605.1:p.Glu224Asp
|
|
NR_037688.3:n.744G>T
|
|
|
NM_001199954.3:c.672G>T
|
NP_001186883.1:p.Glu224Asp
|
|