ENST00000312251.8:c.807A>T
MANE Select
|
ENSP00000310998.3:p.Glu269Asp
|
|
ENST00000649828.1:c.807A>T
|
ENSP00000498032.1:p.Glu269Asp
|
|
ENST00000312251.7:c.807A>T
|
ENSP00000310998.3:p.Glu269Asp
|
|
ENST00000381955.7:c.807A>T
|
ENSP00000371381.3:p.Glu269Asp
|
|
ENST00000562037.1:c.568A>T
|
ENSP00000464994.1:n.568A>T
|
|
ENST00000562346.2:c.505-808A>T
|
|
|
ENST00000562746.5:c.807A>T
|
ENSP00000455900.1:p.Glu269Asp
|
|
ENST00000563578.5:c.625A>T
|
|
|
ENST00000564397.5:n.1166A>T
|
|
|
ENST00000565876.5:c.480+1392A>T
|
|
|
ENST00000567739.5:n.126A>T
|
|
|
ENST00000568202.5:n.670A>T
|
|
|
ENST00000569296.5:c.351A>T
|
ENSP00000465949.1:p.Glu117Asp
|
|
NM_016256.3:c.807A>T
|
NP_057340.2:p.Glu269Asp
|
|
XM_011522517.1:c.807A>T
|
XP_011520819.1:p.Glu269Asp
|
|
XM_011522518.1:c.807A>T
|
XP_011520820.1:p.Glu269Asp
|
|
XM_011522519.1:c.807A>T
|
XP_011520821.1:p.Glu269Asp
|
|
XR_243285.1:n.834A>T
|
|
|
XM_011522517.3:c.807A>T
|
XP_011520819.1:p.Glu269Asp
|
|
XR_001751908.2:n.833A>T
|
|
|
XR_001751909.2:n.833A>T
|
|
|
XR_001751910.2:n.833A>T
|
|
|
XR_001751911.2:n.833A>T
|
|
|
XR_001751912.2:n.833A>T
|
|
|
NM_016256.4:c.807A>T
MANE Select
|
NP_057340.2:p.Glu269Asp
|
|