ENST00000356839.10:c.1335A>T
MANE Select
|
ENSP00000349297.5:p.Glu445Asp
|
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ENST00000322910.9:c.*1290A>T
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ENSP00000325395.5:n.*1290A>T
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|
ENST00000350303.9:c.1269A>T
|
ENSP00000344152.5:p.Glu423Asp
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|
ENST00000356839.9:c.1335A>T
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ENSP00000349297.5:p.Glu445Asp
|
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ENST00000542255.6:c.193A>T
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|
|
ENST00000543245.6:c.1404A>T
|
ENSP00000438689.2:p.Glu468Asp
|
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ENST00000578711.1:n.466A>T
|
|
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ENST00000579425.5:n.451A>T
|
|
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ENST00000579546.1:c.172A>T
|
|
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ENST00000579894.5:n.46A>T
|
|
|
ENST00000583074.5:n.54A>T
|
|
|
ENST00000583850.5:n.110A>T
|
|
|
ENST00000583858.5:c.364A>T
|
|
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ENST00000585203.6:n.526A>T
|
|
|
NM_000018.3:c.1335A>T
|
NP_000009.1:p.Glu445Asp
|
|
NM_001033859.2:c.1269A>T
|
NP_001029031.1:p.Glu423Asp
|
|
NM_001270447.1:c.1404A>T
|
NP_001257376.1:p.Glu468Asp
|
|
NM_001270448.1:c.1107A>T
|
NP_001257377.1:p.Glu369Asp
|
|
XM_006721516.2:c.1335A>T
|
XP_006721579.2:p.Glu445Asp
|
|
XM_011523829.1:c.1335A>T
|
XP_011522131.1:p.Glu445Asp
|
|
XM_011523830.1:c.1335A>T
|
XP_011522132.1:p.Glu445Asp
|
|
XR_934021.1:n.1442A>T
|
|
|
XR_934022.1:n.1442A>T
|
|
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XR_934023.1:n.1442A>T
|
|
|
XM_006721516.3:c.1335A>T
|
XP_006721579.2:p.Glu445Asp
|
|
XM_011523829.2:c.1335A>T
|
XP_011522131.1:p.Glu445Asp
|
|
XM_011523830.2:c.1335A>T
|
XP_011522132.1:p.Glu445Asp
|
|
XM_024450741.1:c.1335A>T
|
XP_024306509.1:p.Glu445Asp
|
|
XR_934021.2:n.1394A>T
|
|
|
XR_934022.2:n.1394A>T
|
|
|
XR_934023.2:n.1394A>T
|
|
|
NM_000018.4:c.1335A>T
MANE Select
|
NP_000009.1:p.Glu445Asp
|
|
NM_001033859.3:c.1269A>T
|
NP_001029031.1:p.Glu423Asp
|
|
NM_001270447.2:c.1404A>T
|
NP_001257376.1:p.Glu468Asp
|
|
NM_001270448.2:c.1107A>T
|
NP_001257377.1:p.Glu369Asp
|
|