ENST00000356839.10:c.291G>T
MANE Select
|
ENSP00000349297.5:p.Glu97Asp
|
|
ENST00000322910.9:c.*246G>T
|
ENSP00000325395.5:n.*246G>T
|
|
ENST00000350303.9:c.225G>T
|
ENSP00000344152.5:p.Glu75Asp
|
|
ENST00000356839.9:c.291G>T
|
ENSP00000349297.5:p.Glu97Asp
|
|
ENST00000543245.6:c.360G>T
|
ENSP00000438689.2:p.Glu120Asp
|
|
ENST00000577191.5:n.368G>T
|
|
|
ENST00000577433.5:n.499G>T
|
|
|
ENST00000577857.5:n.242G>T
|
|
|
ENST00000579286.5:n.472G>T
|
|
|
ENST00000579886.2:c.202-166G>T
|
ENSP00000463246.1:n.202-166G>T
|
|
ENST00000580263.5:n.544G>T
|
|
|
ENST00000580365.1:n.22G>T
|
|
|
ENST00000581562.5:n.338G>T
|
|
|
ENST00000582056.5:n.381G>T
|
|
|
ENST00000582166.1:n.179G>T
|
|
|
ENST00000582356.5:n.490G>T
|
|
|
ENST00000583312.5:c.291G>T
|
ENSP00000467920.1:p.Glu97Asp
|
|
ENST00000584103.5:c.291G>T
|
ENSP00000465353.1:p.Glu97Asp
|
|
NM_000018.3:c.291G>T
|
NP_000009.1:p.Glu97Asp
|
|
NM_001033859.2:c.225G>T
|
NP_001029031.1:p.Glu75Asp
|
|
NM_001270447.1:c.360G>T
|
NP_001257376.1:p.Glu120Asp
|
|
NM_001270448.1:c.63G>T
|
NP_001257377.1:p.Glu21Asp
|
|
XM_006721516.2:c.291G>T
|
XP_006721579.2:p.Glu97Asp
|
|
XM_011523829.1:c.291G>T
|
XP_011522131.1:p.Glu97Asp
|
|
XM_011523830.1:c.291G>T
|
XP_011522132.1:p.Glu97Asp
|
|
XR_934021.1:n.398G>T
|
|
|
XR_934022.1:n.398G>T
|
|
|
XR_934023.1:n.398G>T
|
|
|
XM_006721516.3:c.291G>T
|
XP_006721579.2:p.Glu97Asp
|
|
XM_011523829.2:c.291G>T
|
XP_011522131.1:p.Glu97Asp
|
|
XM_011523830.2:c.291G>T
|
XP_011522132.1:p.Glu97Asp
|
|
XM_024450741.1:c.291G>T
|
XP_024306509.1:p.Glu97Asp
|
|
XR_934021.2:n.350G>T
|
|
|
XR_934022.2:n.350G>T
|
|
|
XR_934023.2:n.350G>T
|
|
|
NM_000018.4:c.291G>T
MANE Select
|
NP_000009.1:p.Glu97Asp
|
|
NM_001033859.3:c.225G>T
|
NP_001029031.1:p.Glu75Asp
|
|
NM_001270447.2:c.360G>T
|
NP_001257376.1:p.Glu120Asp
|
|
NM_001270448.2:c.63G>T
|
NP_001257377.1:p.Glu21Asp
|
|