|
ENST00000555203.6:n.467A=
|
|
|
|
ENST00000619722.5:c.522A=
|
ENSP00000481936.1:p.Glu174=
|
|
|
ENST00000650845.1:n.1323A=
|
|
|
|
ENST00000650904.1:c.777A=
|
ENSP00000498606.1:p.Glu259=
|
|
|
ENST00000651937.1:c.732A=
|
ENSP00000498785.1:p.Glu244=
|
|
|
ENST00000652120.1:n.683A=
|
|
|
|
ENST00000652326.2:c.777A=
MANE Select
|
ENSP00000498929.1:p.Glu259=
|
|
|
ENST00000652732.1:c.*343A=
|
ENSP00000498799.1:n.*343A=
|
|
|
ENST00000674802.1:n.1009A=
|
|
|
|
ENST00000261244.9:c.777A=
|
ENSP00000261244.5:p.Glu259=
|
|
|
ENST00000354386.10:c.936A=
|
ENSP00000346359.6:p.Glu312=
|
|
|
ENST00000423743.7:c.645A=
|
ENSP00000399427.3:p.Glu215=
|
|
|
ENST00000538571.6:n.367A=
|
|
|
|
ENST00000555833.5:c.522A=
|
ENSP00000450855.1:p.Glu174=
|
|
|
ENST00000556134.5:c.645A=
|
ENSP00000452351.2:p.Glu215=
|
|
|
ENST00000619416.4:c.732A=
|
ENSP00000478083.1:p.Glu244=
|
|
|
ENST00000619722.4:c.522A=
|
ENSP00000481936.1:p.Glu174=
|
|
|
NM_001244189.1:c.936A=
|
NP_001231118.1:p.Glu312=
|
|
|
NM_001244190.1:c.732A=
|
NP_001231119.1:p.Glu244=
|
|
|
NM_001244191.1:c.522A=
|
NP_001231120.1:p.Glu174=
|
|
|
NM_001244192.1:c.645A=
|
NP_001231121.1:p.Glu215=
|
|
|
NM_001244193.1:c.357A=
|
NP_001231122.1:p.Glu119=
|
|
|
NM_014749.3:c.777A=
|
NP_055564.3:p.Glu259=
|
|
|
NM_001329943.2:c.777A=
|
NP_001316872.1:p.Glu259=
|
|
|
NM_001329944.1:c.777A=
|
NP_001316873.1:p.Glu259=
|
|
|
NM_001329945.1:c.522A=
|
NP_001316874.1:p.Glu174=
|
|
|
NM_001329946.1:c.777A=
|
NP_001316875.1:p.Glu259=
|
|
|
NM_001329947.1:c.777A=
|
NP_001316876.1:p.Glu259=
|
|
|
NM_001364700.1:c.522A=
|
NP_001351629.1:p.Glu174=
|
|
|
NM_001364701.1:c.522A=
|
NP_001351630.1:p.Glu174=
|
|
|
NM_014749.4:c.777A=
|
NP_055564.3:p.Glu259=
|
|
|
XM_024449779.1:c.900A=
|
XP_024305547.1:p.Glu300=
|
|
|
XM_024449780.1:c.777A=
|
XP_024305548.1:p.Glu259=
|
|
|
XM_024449781.1:c.900A=
|
XP_024305549.1:p.Glu300=
|
|
|
XM_024449782.1:c.522A=
|
XP_024305550.1:p.Glu174=
|
|
|
XM_024449783.1:c.522A=
|
XP_024305551.1:p.Glu174=
|
|
|
XM_024449784.1:c.522A=
|
XP_024305552.1:p.Glu174=
|
|
|
XM_024449785.1:c.522A=
|
XP_024305553.1:p.Glu174=
|
|
|
XM_024449787.1:c.381A=
|
XP_024305555.1:p.Glu127=
|
|
|
XM_024449788.1:c.357A=
|
XP_024305556.1:p.Glu119=
|
|
|
XM_024449789.1:c.357A=
|
XP_024305557.1:p.Glu119=
|
|
|
XM_024449791.1:c.777A=
|
XP_024305559.1:p.Glu259=
|
|
|
NM_001244189.2:c.936A=
|
NP_001231118.1:p.Glu312=
|
|
|
NM_001244190.2:c.732A=
|
NP_001231119.1:p.Glu244=
|
|
|
NM_001244192.2:c.645A=
|
NP_001231121.1:p.Glu215=
|
|
|
NM_001329943.3:c.777A=
MANE Select
|
NP_001316872.1:p.Glu259=
|
|
|
NM_001329944.2:c.777A=
|
NP_001316873.1:p.Glu259=
|
|
|
NM_001329945.2:c.522A=
|
NP_001316874.1:p.Glu174=
|
|
|
NM_001329946.2:c.777A=
|
NP_001316875.1:p.Glu259=
|
|
|
NM_001329947.2:c.777A=
|
NP_001316876.1:p.Glu259=
|
|
|
NM_001364701.2:c.522A=
|
NP_001351630.1:p.Glu174=
|
|
|
NM_014749.5:c.777A=
|
NP_055564.3:p.Glu259=
|
|
|
NM_001244191.2:c.522A=
|
NP_001231120.1:p.Glu174=
|
|
|
NM_001244193.2:c.357A=
|
NP_001231122.1:p.Glu119=
|
|
