ENST00000682565.1:c.11516A=
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ENSP00000507671.1:p.Glu3839=
|
|
ENST00000682801.1:c.11167-966A=
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ENSP00000507862.1:n.11167-966A=
|
|
ENST00000682859.1:c.11516A=
|
ENSP00000508222.1:p.Glu3839=
|
|
ENST00000683791.1:c.4602A=
|
|
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ENST00000684460.1:c.8797A=
|
|
|
ENST00000684548.1:c.11516A=
|
ENSP00000507421.1:p.Glu3839=
|
|
ENST00000684590.1:c.5963A=
|
ENSP00000507376.1:p.Glu1988=
|
|
ENST00000684656.1:c.8981A=
|
|
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ENST00000613296.6:c.11897A=
MANE Select
|
ENSP00000482968.1:p.Glu3966=
|
|
ENST00000651057.1:c.2051A=
|
ENSP00000498504.1:p.Glu684=
|
|
ENST00000651434.1:c.3253A=
|
|
|
ENST00000651750.1:c.1260+338A=
|
|
|
ENST00000652487.1:c.3068A=
|
|
|
ENST00000464408.3:n.72A=
|
|
|
ENST00000484298.5:c.11771A=
|
ENSP00000478155.1:p.Glu3924=
|
|
ENST00000613296.4:c.11897A=
|
ENSP00000482968.1:p.Glu3966=
|
|
ENST00000620466.4:n.5700A=
|
|
|
NM_015120.4:c.11900A= , LRG_741t1:c.11900A=
|
NP_055935.4:p.Glu3967=
|
|
NM_001378454.1:c.11897A=
MANE Select
|
NP_001365383.1:p.Glu3966=
|
|