ENST00000697149.1:c.1379G>C
|
ENSP00000513138.1:n.1379G>C
|
|
ENST00000697150.1:c.1437G>C
|
ENSP00000513139.1:n.1437G>C
|
|
ENST00000697151.1:c.1370G>C
|
ENSP00000513140.1:n.1370G>C
|
|
ENST00000697164.1:c.1450G>C
|
ENSP00000513153.1:p.Asp484His
|
|
ENST00000697165.1:c.1237G>C
|
ENSP00000513154.1:p.Asp413His
|
|
ENST00000347310.10:c.1540G>C
MANE Select
|
ENSP00000321345.5:p.Asp514His
|
|
ENST00000637002.1:c.931G>C
|
ENSP00000490340.1:p.Asp311His
|
|
ENST00000347310.9:c.1540G>C
|
ENSP00000321345.5:p.Asp514His
|
|
ENST00000395227.2:c.334G>C
|
ENSP00000378652.2:p.Asp112His
|
|
ENST00000425614.3:c.775G>C
|
ENSP00000387640.2:p.Asp259His
|
|
ENST00000473881.2:c.*366G>C
|
ENSP00000486667.1:n.*366G>C
|
|
NM_144701.2:c.1540G>C
|
NP_653302.2:p.Asp514His
|
|
XM_005270516.2:c.778G>C
|
XP_005270573.1:p.Asp260His
|
|
XM_011540789.1:c.1630G>C
|
XP_011539091.1:p.Asp544His
|
|
XM_011540790.1:c.1540G>C
|
XP_011539092.1:p.Asp514His
|
|
XM_011540791.1:c.1540G>C
|
XP_011539093.1:p.Asp514His
|
|
XM_011540790.3:c.1540G>C
|
XP_011539092.1:p.Asp514His
|
|
XM_011540791.3:c.1540G>C
|
XP_011539093.1:p.Asp514His
|
|
XR_001736993.1:n.1620G>C
|
|
|
NM_144701.3:c.1540G>C
MANE Select
|
NP_653302.2:p.Asp514His
|
|