ENST00000682565.1:c.11671G>T
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ENSP00000507671.1:p.Ala3891Ser
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ENST00000682801.1:c.11167-811G>T
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ENSP00000507862.1:n.11167-811G>T
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ENST00000682859.1:c.11671G>T
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ENSP00000508222.1:p.Ala3891Ser
|
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ENST00000683791.1:c.4757G>T
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|
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ENST00000684460.1:c.8952G>T
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ENST00000684548.1:c.11671G>T
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ENSP00000507421.1:p.Ala3891Ser
|
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ENST00000684590.1:c.6118G>T
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ENSP00000507376.1:p.Ala2040Ser
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ENST00000684656.1:c.9136G>T
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|
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ENST00000613296.6:c.12052G>T
MANE Select
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ENSP00000482968.1:p.Ala4018Ser
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ENST00000651057.1:c.2206G>T
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ENSP00000498504.1:p.Ala736Ser
|
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ENST00000651434.1:c.3408G>T
|
|
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ENST00000651750.1:c.1260+493G>T
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|
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ENST00000652487.1:c.3223G>T
|
|
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ENST00000464408.3:n.227G>T
|
|
|
ENST00000484298.5:c.11926G>T
|
ENSP00000478155.1:p.Ala3976Ser
|
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ENST00000613296.4:c.12052G>T
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ENSP00000482968.1:p.Ala4018Ser
|
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ENST00000620466.4:n.5855G>T
|
|
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NM_015120.4:c.12055G>T , LRG_741t1:c.12055G>T
|
NP_055935.4:p.Ala4019Ser
|
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NM_001378454.1:c.12052G>T
MANE Select
|
NP_001365383.1:p.Ala4018Ser
|
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