ENST00000593767.3:c.855G>T
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ENSP00000470692.3:p.Ala285=
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ENST00000312865.10:c.855G>T
MANE Select
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ENSP00000326767.5:p.Ala285=
|
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ENST00000538643.5:c.216G>T
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ENSP00000437496.1:p.Ala72=
|
|
ENST00000595185.5:c.688+598G>T
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ENSP00000470027.1:n.688+598G>T
|
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ENST00000612791.4:c.761+384G>T
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ENSP00000479851.1:n.761+384G>T
|
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ENST00000612854.4:c.450+1531G>T
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ENSP00000482155.1:n.450+1531G>T
|
|
ENST00000617849.4:c.158-193G>T
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ENSP00000484882.1:n.158-193G>T
|
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ENST00000618715.4:c.158-192G>T
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ENSP00000480731.1:n.158-192G>T
|
|
ENST00000620467.4:c.855G>T
|
ENSP00000482659.1:p.Ala285=
|
|
ENST00000622402.4:c.146-5281G>T
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ENSP00000478074.1:n.146-5281G>T
|
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NM_030973.3:c.855G>T , LRG_368t1:c.855G>T
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NP_112235.2:p.Ala285=
|
|
XM_011527353.1:c.855G>T
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XP_011525655.1:p.Ala285=
|
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NM_001378355.1:c.855G>T
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NP_001365284.1:p.Ala285=
|
|
NM_030973.4:c.855G>T
MANE Select
|
NP_112235.2:p.Ala285=
|
|