ENST00000682565.1:c.11517A>G
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ENSP00000507671.1:p.Glu3839=
|
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ENST00000682801.1:c.11167-965A>G
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ENSP00000507862.1:n.11167-965A>G
|
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ENST00000682859.1:c.11517A>G
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ENSP00000508222.1:p.Glu3839=
|
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ENST00000683791.1:c.4603A>G
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|
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ENST00000684460.1:c.8798A>G
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|
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ENST00000684548.1:c.11517A>G
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ENSP00000507421.1:p.Glu3839=
|
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ENST00000684590.1:c.5964A>G
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ENSP00000507376.1:p.Glu1988=
|
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ENST00000684656.1:c.8982A>G
|
|
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ENST00000613296.6:c.11898A>G
MANE Select
|
ENSP00000482968.1:p.Glu3966=
|
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ENST00000651057.1:c.2052A>G
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ENSP00000498504.1:p.Glu684=
|
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ENST00000651434.1:c.3254A>G
|
|
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ENST00000651750.1:c.1260+339A>G
|
|
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ENST00000652487.1:c.3069A>G
|
|
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ENST00000464408.3:n.73A>G
|
|
|
ENST00000484298.5:c.11772A>G
|
ENSP00000478155.1:p.Glu3924=
|
|
ENST00000613296.4:c.11898A>G
|
ENSP00000482968.1:p.Glu3966=
|
|
ENST00000620466.4:n.5701A>G
|
|
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NM_015120.4:c.11901A>G , LRG_741t1:c.11901A>G
|
NP_055935.4:p.Glu3967=
|
|
NM_001378454.1:c.11898A>G
MANE Select
|
NP_001365383.1:p.Glu3966=
|
|