ENST00000356839.10:c.386A>T
MANE Select
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ENSP00000349297.5:p.Glu129Val
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ENST00000322910.9:c.*341A>T
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ENSP00000325395.5:n.*341A>T
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ENST00000350303.9:c.320A>T
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ENSP00000344152.5:p.Glu107Val
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ENST00000356839.9:c.386A>T
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ENSP00000349297.5:p.Glu129Val
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ENST00000543245.6:c.455A>T
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ENSP00000438689.2:p.Glu152Val
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ENST00000577191.5:n.463A>T
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ENST00000577433.5:n.594A>T
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|
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ENST00000577857.5:n.293+137A>T
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ENST00000579286.5:n.567A>T
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ENST00000579886.2:c.224A>T
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ENSP00000463246.1:p.Glu75Val
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ENST00000580365.1:n.117A>T
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ENST00000581378.5:c.85A>T
|
|
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ENST00000581562.5:n.433A>T
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ENST00000582056.5:n.569A>T
|
|
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ENST00000582166.1:n.367A>T
|
|
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ENST00000583312.5:c.386A>T
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ENSP00000467920.1:p.Glu129Val
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ENST00000584103.5:c.419A>T
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ENSP00000465353.1:p.Glu140Val
|
|
NM_000018.3:c.386A>T
|
NP_000009.1:p.Glu129Val
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NM_001033859.2:c.320A>T
|
NP_001029031.1:p.Glu107Val
|
|
NM_001270447.1:c.455A>T
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NP_001257376.1:p.Glu152Val
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NM_001270448.1:c.158A>T
|
NP_001257377.1:p.Glu53Val
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XM_006721516.2:c.386A>T
|
XP_006721579.2:p.Glu129Val
|
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XM_011523829.1:c.386A>T
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XP_011522131.1:p.Glu129Val
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XM_011523830.1:c.386A>T
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XP_011522132.1:p.Glu129Val
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XR_934021.1:n.493A>T
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XR_934022.1:n.493A>T
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XR_934023.1:n.493A>T
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|
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XM_006721516.3:c.386A>T
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XP_006721579.2:p.Glu129Val
|
|
XM_011523829.2:c.386A>T
|
XP_011522131.1:p.Glu129Val
|
|
XM_011523830.2:c.386A>T
|
XP_011522132.1:p.Glu129Val
|
|
XM_024450741.1:c.386A>T
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XP_024306509.1:p.Glu129Val
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XR_934021.2:n.445A>T
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|
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XR_934022.2:n.445A>T
|
|
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XR_934023.2:n.445A>T
|
|
|
NM_000018.4:c.386A>T
MANE Select
|
NP_000009.1:p.Glu129Val
|
|
NM_001033859.3:c.320A>T
|
NP_001029031.1:p.Glu107Val
|
|
NM_001270447.2:c.455A>T
|
NP_001257376.1:p.Glu152Val
|
|
NM_001270448.2:c.158A>T
|
NP_001257377.1:p.Glu53Val
|
|