ENST00000682565.1:c.11675G>T
|
ENSP00000507671.1:p.Gly3892Val
|
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ENST00000682801.1:c.11167-807G>T
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ENSP00000507862.1:n.11167-807G>T
|
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ENST00000682859.1:c.11675G>T
|
ENSP00000508222.1:p.Gly3892Val
|
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ENST00000683791.1:c.4761G>T
|
|
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ENST00000684460.1:c.8956G>T
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|
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ENST00000684548.1:c.11675G>T
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ENSP00000507421.1:p.Gly3892Val
|
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ENST00000684590.1:c.6122G>T
|
ENSP00000507376.1:p.Gly2041Val
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ENST00000684656.1:c.9140G>T
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ENST00000613296.6:c.12056G>T
MANE Select
|
ENSP00000482968.1:p.Gly4019Val
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ENST00000651057.1:c.2210G>T
|
ENSP00000498504.1:p.Gly737Val
|
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ENST00000651434.1:c.3412G>T
|
|
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ENST00000651750.1:c.1260+497G>T
|
|
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ENST00000652487.1:c.3227G>T
|
|
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ENST00000464408.3:n.231G>T
|
|
|
ENST00000484298.5:c.11930G>T
|
ENSP00000478155.1:p.Gly3977Val
|
|
ENST00000613296.4:c.12056G>T
|
ENSP00000482968.1:p.Gly4019Val
|
|
ENST00000620466.4:n.5859G>T
|
|
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NM_015120.4:c.12059G>T , LRG_741t1:c.12059G>T
|
NP_055935.4:p.Gly4020Val
|
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NM_001378454.1:c.12056G>T
MANE Select
|
NP_001365383.1:p.Gly4019Val
|
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