ENST00000470094.2:c.8840A>T
|
ENSP00000434898.2:p.Glu2947Val
|
|
ENST00000528762.2:c.*207A>T
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ENSP00000433168.2:n.*207A>T
|
|
ENST00000530893.7:c.8471A>T
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ENSP00000499438.2:p.Glu2824Val
|
|
ENST00000665585.2:c.*402A>T
|
ENSP00000499570.2:n.*402A>T
|
|
ENST00000666593.2:c.8840A>T
|
ENSP00000499256.2:p.Glu2947Val
|
|
ENST00000700202.2:c.8840A>T
|
ENSP00000514856.2:p.Glu2947Val
|
|
ENST00000700202.1:c.1307A>T
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ENSP00000514856.1:p.Glu436Val
|
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ENST00000700203.1:n.967A>T
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|
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ENST00000380152.8:c.8840A>T
MANE Select
|
ENSP00000369497.3:p.Glu2947Val
|
|
ENST00000544455.6:c.8840A>T
|
ENSP00000439902.1:p.Glu2947Val
|
|
ENST00000614259.2:c.8848A>T
|
ENSP00000506251.1:n.8848A>T
|
|
ENST00000665585.1:c.1718A>T
|
|
|
ENST00000680887.1:c.8840A>T
|
ENSP00000505508.1:p.Glu2947Val
|
|
ENST00000380152.7:c.8840A>T
|
ENSP00000369497.3:p.Glu2947Val
|
|
ENST00000528762.1:c.402A>T
|
ENSP00000433168.1:n.402A>T
|
|
ENST00000544455.5:c.8840A>T
|
ENSP00000439902.1:p.Glu2947Val
|
|
NM_000059.3:c.8840A>T , LRG_293t1:c.8840A>T
|
NP_000050.2:p.Glu2947Val
|
|
XM_011535203.1:c.8840A>T
|
XP_011533505.1:p.Glu2947Val
|
|
XM_011535204.1:c.8744A>T
|
XP_011533506.1:p.Glu2915Val
|
|
XM_011535205.1:c.8755-348A>T
|
XP_011533507.1:n.8755-348A>T
|
|
NM_000059.4:c.8840A>T
MANE Select
|
NP_000050.3:p.Glu2947Val
|
|