ENST00000682114.1:c.434A>T
|
ENSP00000507245.1:p.Glu145Val
|
|
ENST00000682478.1:n.624A>T
|
|
|
ENST00000683576.1:n.624A>T
|
|
|
ENST00000683627.1:c.434A>T
|
ENSP00000507533.1:p.Glu145Val
|
|
ENST00000684082.1:c.391A>T
|
ENSP00000508266.1:n.391A>T
|
|
ENST00000684633.1:n.406A>T
|
|
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ENST00000684678.1:c.430A>T
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ENSP00000507059.1:n.430A>T
|
|
ENST00000369842.9:c.434A>T
MANE Select
|
ENSP00000358857.4:p.Glu145Val
|
|
ENST00000369835.3:c.329A>T
|
ENSP00000358850.3:p.Glu110Val
|
|
ENST00000369842.8:c.434A>T
|
ENSP00000358857.4:p.Glu145Val
|
|
ENST00000428228.5:c.*339A>T
|
ENSP00000401081.1:n.*339A>T
|
|
ENST00000468294.5:n.394A>T
|
|
|
ENST00000471965.1:n.223A>T
|
|
|
ENST00000485261.1:n.624A>T
|
|
|
ENST00000486738.5:n.792A>T
|
|
|
ENST00000492448.1:n.417A>T
|
|
|
NM_000117.2:c.434A>T , LRG_745t1:c.434A>T
|
NP_000108.1:p.Glu145Val
|
|
XM_024452349.1:c.440A>T
|
XP_024308117.1:p.Glu147Val
|
|
NM_000117.3:c.434A>T
MANE Select
|
NP_000108.1:p.Glu145Val
|
|