ENST00000539215.6:c.132A>G
|
|
|
ENST00000545015.2:n.1451A>G
|
|
|
ENST00000699982.1:c.1278A>G
|
|
|
ENST00000699983.1:c.1278A>G
|
|
|
ENST00000699984.1:c.1278A>G
|
|
|
ENST00000320574.10:c.1424A>G
MANE Select
|
ENSP00000322570.5:p.His475Arg
|
|
ENST00000672742.1:c.*926A>G
|
ENSP00000500279.1:n.*926A>G
|
|
ENST00000320574.9:c.1424A>G
|
ENSP00000322570.5:p.His475Arg
|
|
ENST00000535270.5:c.1343A>G
|
ENSP00000445753.1:p.His448Arg
|
|
ENST00000535934.2:n.1299A>G
|
|
|
ENST00000537064.5:c.*471A>G
|
ENSP00000442578.1:n.*471A>G
|
|
ENST00000539215.5:n.132A>G
|
|
|
ENST00000545015.1:n.21A>G
|
|
|
NM_006231.3:c.1424A>G , LRG_789t1:c.1424A>G
|
NP_006222.2:p.His475Arg
|
|
XM_011534795.1:c.1424A>G
|
XP_011533097.1:p.His475Arg
|
|
XM_011534796.1:c.1295A>G
|
XP_011533098.1:p.His432Arg
|
|
XM_011534797.1:c.503A>G
|
XP_011533099.1:p.His168Arg
|
|
XM_011534798.1:c.86A>G
|
XP_011533100.1:p.His29Arg
|
|
XM_011534799.1:c.1424A>G
|
XP_011533101.1:p.His475Arg
|
|
XM_011534800.1:c.1424A>G
|
XP_011533102.1:p.His475Arg
|
|
XM_011534801.1:c.1424A>G
|
XP_011533103.1:p.His475Arg
|
|
XR_941395.1:n.1633A>G
|
|
|
XM_011534795.3:c.1424A>G
|
XP_011533097.1:p.His475Arg
|
|
XM_011534797.3:c.503A>G
|
XP_011533099.1:p.His168Arg
|
|
XM_011534799.2:c.1424A>G
|
XP_011533101.1:p.His475Arg
|
|
XR_002957338.1:n.1628A>G
|
|
|
XR_002957339.1:n.1628A>G
|
|
|
XR_941395.2:n.1628A>G
|
|
|
NM_006231.4:c.1424A>G
MANE Select
|
NP_006222.2:p.His475Arg
|
|