ENST00000392334.7:c.101A>T
|
ENSP00000376146.2:p.Glu34Val
|
|
ENST00000314028.11:c.101A>T
MANE Select
|
ENSP00000324464.6:p.Glu34Val
|
|
ENST00000314028.10:c.101A>T
|
ENSP00000324464.6:p.Glu34Val
|
|
ENST00000392334.6:c.101A>T
|
ENSP00000376146.2:p.Glu34Val
|
|
ENST00000398519.9:c.101A>T
|
ENSP00000381531.5:p.Glu34Val
|
|
ENST00000403276.7:c.101A>T
|
ENSP00000385769.3:p.Glu34Val
|
|
ENST00000578194.5:n.307A>T
|
|
|
ENST00000579308.1:n.126A>T
|
|
|
ENST00000579316.5:n.158A>T
|
|
|
ENST00000580061.5:n.101A>T
|
|
|
ENST00000580446.1:c.76+7534A>T
|
ENSP00000463757.1:n.76+7534A>T
|
|
ENST00000581241.5:n.89A>T
|
|
|
ENST00000581660.5:c.*139A>T
|
ENSP00000464551.1:n.*139A>T
|
|
ENST00000582844.5:n.59A>T
|
|
|
ENST00000584472.5:n.186A>T
|
|
|
ENST00000585026.1:c.*147A>T
|
ENSP00000462144.1:n.*147A>T
|
|
NM_001893.4:c.101A>T
|
NP_001884.2:p.Glu34Val
|
|
NM_139062.2:c.101A>T
|
NP_620693.1:p.Glu34Val
|
|
NR_110578.1:n.462A>T
|
|
|
XM_005256336.2:c.101A>T
|
XP_005256393.1:p.Glu34Val
|
|
XM_005256337.3:c.101A>T
|
XP_005256394.1:p.Glu34Val
|
|
XR_243518.2:n.421A>T
|
|
|
XR_430028.2:n.421A>T
|
|
|
XR_933922.1:n.421A>T
|
|
|
XR_933923.1:n.421A>T
|
|
|
NM_001363749.1:c.101A>T
|
NP_001350678.1:p.Glu34Val
|
|
NM_001893.5:c.101A>T
|
NP_001884.2:p.Glu34Val
|
|
NM_139062.3:c.101A>T
|
NP_620693.1:p.Glu34Val
|
|
NR_110578.2:n.470A>T
|
|
|
XM_005256336.4:c.101A>T
|
XP_005256393.1:p.Glu34Val
|
|
XR_002957961.1:n.420A>T
|
|
|
XR_243518.4:n.420A>T
|
|
|
XR_430028.4:n.420A>T
|
|
|
XR_933922.3:n.420A>T
|
|
|
XR_933923.3:n.420A>T
|
|
|
NM_001363749.2:c.101A>T
|
NP_001350678.1:p.Glu34Val
|
|
NM_001893.6:c.101A>T
MANE Select
|
NP_001884.2:p.Glu34Val
|
|
NM_139062.4:c.101A>T
|
NP_620693.1:p.Glu34Val
|
|