ENST00000356839.10:c.447G>T
MANE Select
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ENSP00000349297.5:p.Glu149Asp
|
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ENST00000322910.9:c.*402G>T
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ENSP00000325395.5:n.*402G>T
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|
ENST00000350303.9:c.381G>T
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ENSP00000344152.5:p.Glu127Asp
|
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ENST00000356839.9:c.447G>T
|
ENSP00000349297.5:p.Glu149Asp
|
|
ENST00000543245.6:c.516G>T
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ENSP00000438689.2:p.Glu172Asp
|
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ENST00000577191.5:n.524G>T
|
|
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ENST00000577433.5:n.655G>T
|
|
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ENST00000577857.5:n.293+198G>T
|
|
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ENST00000579286.5:n.628G>T
|
|
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ENST00000579886.2:c.285G>T
|
ENSP00000463246.1:p.Glu95Asp
|
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ENST00000580365.1:n.178G>T
|
|
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ENST00000581378.5:c.146G>T
|
|
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ENST00000581562.5:n.494G>T
|
|
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ENST00000582056.5:n.630G>T
|
|
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ENST00000582166.1:n.428G>T
|
|
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ENST00000583312.5:c.447G>T
|
ENSP00000467920.1:p.Glu149Asp
|
|
NM_000018.3:c.447G>T
|
NP_000009.1:p.Glu149Asp
|
|
NM_001033859.2:c.381G>T
|
NP_001029031.1:p.Glu127Asp
|
|
NM_001270447.1:c.516G>T
|
NP_001257376.1:p.Glu172Asp
|
|
NM_001270448.1:c.219G>T
|
NP_001257377.1:p.Glu73Asp
|
|
XM_006721516.2:c.447G>T
|
XP_006721579.2:p.Glu149Asp
|
|
XM_011523829.1:c.447G>T
|
XP_011522131.1:p.Glu149Asp
|
|
XM_011523830.1:c.447G>T
|
XP_011522132.1:p.Glu149Asp
|
|
XR_934021.1:n.554G>T
|
|
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XR_934022.1:n.554G>T
|
|
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XR_934023.1:n.554G>T
|
|
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XM_006721516.3:c.447G>T
|
XP_006721579.2:p.Glu149Asp
|
|
XM_011523829.2:c.447G>T
|
XP_011522131.1:p.Glu149Asp
|
|
XM_011523830.2:c.447G>T
|
XP_011522132.1:p.Glu149Asp
|
|
XM_024450741.1:c.447G>T
|
XP_024306509.1:p.Glu149Asp
|
|
XR_934021.2:n.506G>T
|
|
|
XR_934022.2:n.506G>T
|
|
|
XR_934023.2:n.506G>T
|
|
|
NM_000018.4:c.447G>T
MANE Select
|
NP_000009.1:p.Glu149Asp
|
|
NM_001033859.3:c.381G>T
|
NP_001029031.1:p.Glu127Asp
|
|
NM_001270447.2:c.516G>T
|
NP_001257376.1:p.Glu172Asp
|
|
NM_001270448.2:c.219G>T
|
NP_001257377.1:p.Glu73Asp
|
|