ENST00000682565.1:c.11635T>G
|
ENSP00000507671.1:p.Cys3879Gly
|
|
ENST00000682801.1:c.11167-847T>G
|
ENSP00000507862.1:n.11167-847T>G
|
|
ENST00000682859.1:c.11635T>G
|
ENSP00000508222.1:p.Cys3879Gly
|
|
ENST00000683791.1:c.4721T>G
|
|
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ENST00000684460.1:c.8916T>G
|
|
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ENST00000684548.1:c.11635T>G
|
ENSP00000507421.1:p.Cys3879Gly
|
|
ENST00000684590.1:c.6082T>G
|
ENSP00000507376.1:p.Cys2028Gly
|
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ENST00000684656.1:c.9100T>G
|
|
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ENST00000613296.6:c.12016T>G
MANE Select
|
ENSP00000482968.1:p.Cys4006Gly
|
|
ENST00000651057.1:c.2170T>G
|
ENSP00000498504.1:p.Cys724Gly
|
|
ENST00000651434.1:c.3372T>G
|
|
|
ENST00000651750.1:c.1260+457T>G
|
|
|
ENST00000652487.1:c.3187T>G
|
|
|
ENST00000464408.3:n.191T>G
|
|
|
ENST00000484298.5:c.11890T>G
|
ENSP00000478155.1:p.Cys3964Gly
|
|
ENST00000613296.4:c.12016T>G
|
ENSP00000482968.1:p.Cys4006Gly
|
|
ENST00000620466.4:n.5819T>G
|
|
|
NM_015120.4:c.12019T>G , LRG_741t1:c.12019T>G
|
NP_055935.4:p.Cys4007Gly
|
|
NM_001378454.1:c.12016T>G
MANE Select
|
NP_001365383.1:p.Cys4006Gly
|
|