ENST00000699982.1:c.2079G>A
|
|
|
ENST00000699983.1:c.2079G>A
|
|
|
ENST00000699984.1:c.2079G>A
|
|
|
ENST00000320574.10:c.2225G>A
MANE Select
|
ENSP00000322570.5:p.Arg742His
|
|
ENST00000672742.1:c.*1727G>A
|
ENSP00000500279.1:n.*1727G>A
|
|
ENST00000320574.9:c.2225G>A
|
ENSP00000322570.5:p.Arg742His
|
|
ENST00000535270.5:c.2144G>A
|
ENSP00000445753.1:p.Arg715His
|
|
ENST00000537064.5:c.*1272G>A
|
ENSP00000442578.1:n.*1272G>A
|
|
NM_006231.3:c.2225G>A , LRG_789t1:c.2225G>A
|
NP_006222.2:p.Arg742His
|
|
XM_011534795.1:c.2225G>A
|
XP_011533097.1:p.Arg742His
|
|
XM_011534796.1:c.2096G>A
|
XP_011533098.1:p.Arg699His
|
|
XM_011534797.1:c.1304G>A
|
XP_011533099.1:p.Arg435His
|
|
XM_011534798.1:c.887G>A
|
XP_011533100.1:p.Arg296His
|
|
XM_011534799.1:c.2225G>A
|
XP_011533101.1:p.Arg742His
|
|
XM_011534800.1:c.2225G>A
|
XP_011533102.1:p.Arg742His
|
|
XM_011534801.1:c.2225G>A
|
XP_011533103.1:p.Arg742His
|
|
XR_941395.1:n.2434G>A
|
|
|
XM_011534795.3:c.2225G>A
|
XP_011533097.1:p.Arg742His
|
|
XM_011534797.3:c.1304G>A
|
XP_011533099.1:p.Arg435His
|
|
XM_011534799.2:c.2225G>A
|
XP_011533101.1:p.Arg742His
|
|
XR_002957338.1:n.2429G>A
|
|
|
XR_002957339.1:n.2429G>A
|
|
|
XR_941395.2:n.2429G>A
|
|
|
NM_006231.4:c.2225G>A
MANE Select
|
NP_006222.2:p.Arg742His
|
|