ENST00000356839.10:c.1643A>T
MANE Select
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ENSP00000349297.5:p.Glu548Val
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ENST00000322910.9:c.*1598A>T
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ENSP00000325395.5:n.*1598A>T
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|
ENST00000350303.9:c.1577A>T
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ENSP00000344152.5:p.Glu526Val
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ENST00000356839.9:c.1643A>T
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ENSP00000349297.5:p.Glu548Val
|
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ENST00000542255.6:c.501A>T
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|
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ENST00000543245.6:c.1712A>T
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ENSP00000438689.2:p.Glu571Val
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ENST00000578319.5:n.224A>T
|
|
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ENST00000578711.1:n.1013A>T
|
|
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ENST00000578809.5:n.215A>T
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|
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ENST00000579391.1:n.247A>T
|
|
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ENST00000579425.5:n.759A>T
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|
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ENST00000579546.1:c.378A>T
|
|
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ENST00000582450.1:n.151A>T
|
|
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ENST00000583074.5:n.264A>T
|
|
|
ENST00000583848.5:c.29A>T
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ENSP00000466487.1:p.Glu10Val
|
|
ENST00000583850.5:n.414A>T
|
|
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ENST00000583858.5:c.574A>T
|
|
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ENST00000585203.6:n.834A>T
|
|
|
NM_000018.3:c.1643A>T
|
NP_000009.1:p.Glu548Val
|
|
NM_001033859.2:c.1577A>T
|
NP_001029031.1:p.Glu526Val
|
|
NM_001270447.1:c.1712A>T
|
NP_001257376.1:p.Glu571Val
|
|
NM_001270448.1:c.1415A>T
|
NP_001257377.1:p.Glu472Val
|
|
XM_006721516.2:c.1643A>T
|
XP_006721579.2:p.Glu548Val
|
|
XM_011523829.1:c.1541A>T
|
XP_011522131.1:p.Glu514Val
|
|
XM_011523830.1:c.1541A>T
|
XP_011522132.1:p.Glu514Val
|
|
XR_934021.1:n.1746A>T
|
|
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XR_934022.1:n.1652A>T
|
|
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XR_934023.1:n.1652A>T
|
|
|
XM_006721516.3:c.1643A>T
|
XP_006721579.2:p.Glu548Val
|
|
XM_011523829.2:c.1541A>T
|
XP_011522131.1:p.Glu514Val
|
|
XM_011523830.2:c.1541A>T
|
XP_011522132.1:p.Glu514Val
|
|
XM_024450741.1:c.1631A>T
|
XP_024306509.1:p.Glu544Val
|
|
XR_934021.2:n.1698A>T
|
|
|
XR_934022.2:n.1604A>T
|
|
|
XR_934023.2:n.1604A>T
|
|
|
NM_000018.4:c.1643A>T
MANE Select
|
NP_000009.1:p.Glu548Val
|
|
NM_001033859.3:c.1577A>T
|
NP_001029031.1:p.Glu526Val
|
|
NM_001270447.2:c.1712A>T
|
NP_001257376.1:p.Glu571Val
|
|
NM_001270448.2:c.1415A>T
|
NP_001257377.1:p.Glu472Val
|
|