ENST00000682565.1:c.11615A>T
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ENSP00000507671.1:p.Glu3872Val
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ENST00000682801.1:c.11167-867A>T
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ENSP00000507862.1:n.11167-867A>T
|
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ENST00000682859.1:c.11615A>T
|
ENSP00000508222.1:p.Glu3872Val
|
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ENST00000683791.1:c.4701A>T
|
|
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ENST00000684460.1:c.8896A>T
|
|
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ENST00000684548.1:c.11615A>T
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ENSP00000507421.1:p.Glu3872Val
|
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ENST00000684590.1:c.6062A>T
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ENSP00000507376.1:p.Glu2021Val
|
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ENST00000684656.1:c.9080A>T
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|
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ENST00000613296.6:c.11996A>T
MANE Select
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ENSP00000482968.1:p.Glu3999Val
|
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ENST00000651057.1:c.2150A>T
|
ENSP00000498504.1:p.Glu717Val
|
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ENST00000651434.1:c.3352A>T
|
|
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ENST00000651750.1:c.1260+437A>T
|
|
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ENST00000652487.1:c.3167A>T
|
|
|
ENST00000464408.3:n.171A>T
|
|
|
ENST00000484298.5:c.11870A>T
|
ENSP00000478155.1:p.Glu3957Val
|
|
ENST00000613296.4:c.11996A>T
|
ENSP00000482968.1:p.Glu3999Val
|
|
ENST00000620466.4:n.5799A>T
|
|
|
NM_015120.4:c.11999A>T , LRG_741t1:c.11999A>T
|
NP_055935.4:p.Glu4000Val
|
|
NM_001378454.1:c.11996A>T
MANE Select
|
NP_001365383.1:p.Glu3999Val
|
|