ENST00000356839.10:c.597A>T
MANE Select
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ENSP00000349297.5:p.Glu199Asp
|
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ENST00000322910.9:c.*552A>T
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ENSP00000325395.5:n.*552A>T
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ENST00000350303.9:c.531A>T
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ENSP00000344152.5:p.Glu177Asp
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ENST00000356839.9:c.597A>T
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ENSP00000349297.5:p.Glu199Asp
|
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ENST00000543245.6:c.666A>T
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ENSP00000438689.2:p.Glu222Asp
|
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ENST00000577191.5:n.674A>T
|
|
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ENST00000577857.5:n.413A>T
|
|
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ENST00000579286.5:n.778A>T
|
|
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ENST00000579886.2:c.435A>T
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ENSP00000463246.1:p.Glu145Asp
|
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ENST00000580365.1:n.328A>T
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|
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ENST00000581378.5:c.315A>T
|
|
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ENST00000581562.5:n.525-295A>T
|
|
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ENST00000583312.5:c.597A>T
|
ENSP00000467920.1:p.Glu199Asp
|
|
ENST00000583760.1:n.379A>T
|
|
|
NM_000018.3:c.597A>T
|
NP_000009.1:p.Glu199Asp
|
|
NM_001033859.2:c.531A>T
|
NP_001029031.1:p.Glu177Asp
|
|
NM_001270447.1:c.666A>T
|
NP_001257376.1:p.Glu222Asp
|
|
NM_001270448.1:c.369A>T
|
NP_001257377.1:p.Glu123Asp
|
|
XM_006721516.2:c.597A>T
|
XP_006721579.2:p.Glu199Asp
|
|
XM_011523829.1:c.597A>T
|
XP_011522131.1:p.Glu199Asp
|
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XM_011523830.1:c.597A>T
|
XP_011522132.1:p.Glu199Asp
|
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XR_934021.1:n.704A>T
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|
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XR_934022.1:n.704A>T
|
|
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XR_934023.1:n.704A>T
|
|
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XM_006721516.3:c.597A>T
|
XP_006721579.2:p.Glu199Asp
|
|
XM_011523829.2:c.597A>T
|
XP_011522131.1:p.Glu199Asp
|
|
XM_011523830.2:c.597A>T
|
XP_011522132.1:p.Glu199Asp
|
|
XM_024450741.1:c.597A>T
|
XP_024306509.1:p.Glu199Asp
|
|
XR_934021.2:n.656A>T
|
|
|
XR_934022.2:n.656A>T
|
|
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XR_934023.2:n.656A>T
|
|
|
NM_000018.4:c.597A>T
MANE Select
|
NP_000009.1:p.Glu199Asp
|
|
NM_001033859.3:c.531A>T
|
NP_001029031.1:p.Glu177Asp
|
|
NM_001270447.2:c.666A>T
|
NP_001257376.1:p.Glu222Asp
|
|
NM_001270448.2:c.369A>T
|
NP_001257377.1:p.Glu123Asp
|
|