ENST00000356839.10:c.1848G>T
MANE Select
|
ENSP00000349297.5:p.Glu616Asp
|
|
ENST00000322910.9:c.*1803G>T
|
ENSP00000325395.5:n.*1803G>T
|
|
ENST00000350303.9:c.1782G>T
|
ENSP00000344152.5:p.Glu594Asp
|
|
ENST00000356839.9:c.1848G>T
|
ENSP00000349297.5:p.Glu616Asp
|
|
ENST00000542255.6:c.727G>T
|
|
|
ENST00000543245.6:c.1917G>T
|
ENSP00000438689.2:p.Glu639Asp
|
|
ENST00000578033.1:n.273G>T
|
|
|
ENST00000578319.5:n.429G>T
|
|
|
ENST00000578711.1:n.1473G>T
|
|
|
ENST00000578809.5:n.420G>T
|
|
|
ENST00000579425.5:n.964G>T
|
|
|
ENST00000583848.5:c.214G>T
|
ENSP00000466487.1:n.214G>T
|
|
ENST00000583850.5:n.619G>T
|
|
|
ENST00000583858.5:c.779G>T
|
|
|
NM_000018.3:c.1848G>T
|
NP_000009.1:p.Glu616Asp
|
|
NM_001033859.2:c.1782G>T
|
NP_001029031.1:p.Glu594Asp
|
|
NM_001270447.1:c.1917G>T
|
NP_001257376.1:p.Glu639Asp
|
|
NM_001270448.1:c.1620G>T
|
NP_001257377.1:p.Glu540Asp
|
|
XM_006721516.2:c.1869G>T
|
XP_006721579.2:p.Glu623Asp
|
|
XM_011523829.1:c.1767G>T
|
XP_011522131.1:p.Glu589Asp
|
|
XM_011523830.1:c.1746G>T
|
XP_011522132.1:p.Glu582Asp
|
|
XR_934021.1:n.1951G>T
|
|
|
XR_934022.1:n.1857G>T
|
|
|
XR_934023.1:n.1878G>T
|
|
|
XM_006721516.3:c.1869G>T
|
XP_006721579.2:p.Glu623Asp
|
|
XM_011523829.2:c.1767G>T
|
XP_011522131.1:p.Glu589Asp
|
|
XM_011523830.2:c.1746G>T
|
XP_011522132.1:p.Glu582Asp
|
|
XM_024450741.1:c.1836G>T
|
XP_024306509.1:p.Glu612Asp
|
|
XR_934021.2:n.1903G>T
|
|
|
XR_934022.2:n.1809G>T
|
|
|
XR_934023.2:n.1830G>T
|
|
|
NM_000018.4:c.1848G>T
MANE Select
|
NP_000009.1:p.Glu616Asp
|
|
NM_001033859.3:c.1782G>T
|
NP_001029031.1:p.Glu594Asp
|
|
NM_001270447.2:c.1917G>T
|
NP_001257376.1:p.Glu639Asp
|
|
NM_001270448.2:c.1620G>T
|
NP_001257377.1:p.Glu540Asp
|
|