ENST00000697149.1:c.1362C>G
|
ENSP00000513138.1:n.1362C>G
|
|
ENST00000697150.1:c.1420C>G
|
ENSP00000513139.1:n.1420C>G
|
|
ENST00000697151.1:c.1353C>G
|
ENSP00000513140.1:n.1353C>G
|
|
ENST00000697164.1:c.1433C>G
|
ENSP00000513153.1:p.Thr478Arg
|
|
ENST00000697165.1:c.1220C>G
|
ENSP00000513154.1:p.Thr407Arg
|
|
ENST00000347310.10:c.1523C>G
MANE Select
|
ENSP00000321345.5:p.Thr508Arg
|
|
ENST00000637002.1:c.914C>G
|
ENSP00000490340.1:p.Thr305Arg
|
|
ENST00000347310.9:c.1523C>G
|
ENSP00000321345.5:p.Thr508Arg
|
|
ENST00000395227.2:c.317C>G
|
ENSP00000378652.2:p.Thr106Arg
|
|
ENST00000425614.3:c.758C>G
|
ENSP00000387640.2:p.Thr253Arg
|
|
ENST00000473881.2:c.*349C>G
|
ENSP00000486667.1:n.*349C>G
|
|
NM_144701.2:c.1523C>G
|
NP_653302.2:p.Thr508Arg
|
|
XM_005270516.2:c.761C>G
|
XP_005270573.1:p.Thr254Arg
|
|
XM_011540789.1:c.1613C>G
|
XP_011539091.1:p.Thr538Arg
|
|
XM_011540790.1:c.1523C>G
|
XP_011539092.1:p.Thr508Arg
|
|
XM_011540791.1:c.1523C>G
|
XP_011539093.1:p.Thr508Arg
|
|
XM_011540790.3:c.1523C>G
|
XP_011539092.1:p.Thr508Arg
|
|
XM_011540791.3:c.1523C>G
|
XP_011539093.1:p.Thr508Arg
|
|
XR_001736993.1:n.1603C>G
|
|
|
NM_144701.3:c.1523C>G
MANE Select
|
NP_653302.2:p.Thr508Arg
|
|