ENST00000682114.1:c.432A>T
|
ENSP00000507245.1:p.Glu144Asp
|
|
ENST00000682478.1:n.622A>T
|
|
|
ENST00000683576.1:n.622A>T
|
|
|
ENST00000683627.1:c.432A>T
|
ENSP00000507533.1:p.Glu144Asp
|
|
ENST00000684082.1:c.389A>T
|
ENSP00000508266.1:n.389A>T
|
|
ENST00000684633.1:n.404A>T
|
|
|
ENST00000684678.1:c.428A>T
|
ENSP00000507059.1:n.428A>T
|
|
ENST00000369842.9:c.432A>T
MANE Select
|
ENSP00000358857.4:p.Glu144Asp
|
|
ENST00000369835.3:c.327A>T
|
ENSP00000358850.3:p.Glu109Asp
|
|
ENST00000369842.8:c.432A>T
|
ENSP00000358857.4:p.Glu144Asp
|
|
ENST00000428228.5:c.*337A>T
|
ENSP00000401081.1:n.*337A>T
|
|
ENST00000468294.5:n.392A>T
|
|
|
ENST00000471965.1:n.221A>T
|
|
|
ENST00000485261.1:n.622A>T
|
|
|
ENST00000486738.5:n.790A>T
|
|
|
ENST00000492448.1:n.415A>T
|
|
|
NM_000117.2:c.432A>T , LRG_745t1:c.432A>T
|
NP_000108.1:p.Glu144Asp
|
|
XM_024452349.1:c.438A>T
|
XP_024308117.1:p.Glu146Asp
|
|
NM_000117.3:c.432A>T
MANE Select
|
NP_000108.1:p.Glu144Asp
|
|