ENST00000682565.1:c.11662G>T
|
ENSP00000507671.1:p.Gly3888Cys
|
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ENST00000682801.1:c.11167-820G>T
|
ENSP00000507862.1:n.11167-820G>T
|
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ENST00000682859.1:c.11662G>T
|
ENSP00000508222.1:p.Gly3888Cys
|
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ENST00000683791.1:c.4748G>T
|
|
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ENST00000684460.1:c.8943G>T
|
|
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ENST00000684548.1:c.11662G>T
|
ENSP00000507421.1:p.Gly3888Cys
|
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ENST00000684590.1:c.6109G>T
|
ENSP00000507376.1:p.Gly2037Cys
|
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ENST00000684656.1:c.9127G>T
|
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ENST00000613296.6:c.12043G>T
MANE Select
|
ENSP00000482968.1:p.Gly4015Cys
|
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ENST00000651057.1:c.2197G>T
|
ENSP00000498504.1:p.Gly733Cys
|
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ENST00000651434.1:c.3399G>T
|
|
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ENST00000651750.1:c.1260+484G>T
|
|
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ENST00000652487.1:c.3214G>T
|
|
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ENST00000464408.3:n.218G>T
|
|
|
ENST00000484298.5:c.11917G>T
|
ENSP00000478155.1:p.Gly3973Cys
|
|
ENST00000613296.4:c.12043G>T
|
ENSP00000482968.1:p.Gly4015Cys
|
|
ENST00000620466.4:n.5846G>T
|
|
|
NM_015120.4:c.12046G>T , LRG_741t1:c.12046G>T
|
NP_055935.4:p.Gly4016Cys
|
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NM_001378454.1:c.12043G>T
MANE Select
|
NP_001365383.1:p.Gly4015Cys
|
|