ENST00000356839.10:c.378G>T
MANE Select
|
ENSP00000349297.5:p.Glu126Asp
|
|
ENST00000322910.9:c.*333G>T
|
ENSP00000325395.5:n.*333G>T
|
|
ENST00000350303.9:c.312G>T
|
ENSP00000344152.5:p.Glu104Asp
|
|
ENST00000356839.9:c.378G>T
|
ENSP00000349297.5:p.Glu126Asp
|
|
ENST00000543245.6:c.447G>T
|
ENSP00000438689.2:p.Glu149Asp
|
|
ENST00000577191.5:n.455G>T
|
|
|
ENST00000577433.5:n.586G>T
|
|
|
ENST00000577857.5:n.293+129G>T
|
|
|
ENST00000579286.5:n.559G>T
|
|
|
ENST00000579886.2:c.216G>T
|
ENSP00000463246.1:p.Glu72Asp
|
|
ENST00000580365.1:n.109G>T
|
|
|
ENST00000581378.5:c.77G>T
|
|
|
ENST00000581562.5:n.425G>T
|
|
|
ENST00000582056.5:n.561G>T
|
|
|
ENST00000582166.1:n.359G>T
|
|
|
ENST00000583312.5:c.378G>T
|
ENSP00000467920.1:p.Glu126Asp
|
|
ENST00000584103.5:c.411G>T
|
ENSP00000465353.1:p.Glu137Asp
|
|
NM_000018.3:c.378G>T
|
NP_000009.1:p.Glu126Asp
|
|
NM_001033859.2:c.312G>T
|
NP_001029031.1:p.Glu104Asp
|
|
NM_001270447.1:c.447G>T
|
NP_001257376.1:p.Glu149Asp
|
|
NM_001270448.1:c.150G>T
|
NP_001257377.1:p.Glu50Asp
|
|
XM_006721516.2:c.378G>T
|
XP_006721579.2:p.Glu126Asp
|
|
XM_011523829.1:c.378G>T
|
XP_011522131.1:p.Glu126Asp
|
|
XM_011523830.1:c.378G>T
|
XP_011522132.1:p.Glu126Asp
|
|
XR_934021.1:n.485G>T
|
|
|
XR_934022.1:n.485G>T
|
|
|
XR_934023.1:n.485G>T
|
|
|
XM_006721516.3:c.378G>T
|
XP_006721579.2:p.Glu126Asp
|
|
XM_011523829.2:c.378G>T
|
XP_011522131.1:p.Glu126Asp
|
|
XM_011523830.2:c.378G>T
|
XP_011522132.1:p.Glu126Asp
|
|
XM_024450741.1:c.378G>T
|
XP_024306509.1:p.Glu126Asp
|
|
XR_934021.2:n.437G>T
|
|
|
XR_934022.2:n.437G>T
|
|
|
XR_934023.2:n.437G>T
|
|
|
NM_000018.4:c.378G>T
MANE Select
|
NP_000009.1:p.Glu126Asp
|
|
NM_001033859.3:c.312G>T
|
NP_001029031.1:p.Glu104Asp
|
|
NM_001270447.2:c.447G>T
|
NP_001257376.1:p.Glu149Asp
|
|
NM_001270448.2:c.150G>T
|
NP_001257377.1:p.Glu50Asp
|
|