ENST00000697149.1:c.1544G>T
|
ENSP00000513138.1:n.1544G>T
|
|
ENST00000697150.1:c.1602G>T
|
ENSP00000513139.1:n.1602G>T
|
|
ENST00000697151.1:c.1535G>T
|
ENSP00000513140.1:n.1535G>T
|
|
ENST00000697164.1:c.1615G>T
|
ENSP00000513153.1:p.Glu539Ter
|
|
ENST00000697165.1:c.1402G>T
|
ENSP00000513154.1:p.Glu468Ter
|
|
ENST00000347310.10:c.1705G>T
MANE Select
|
ENSP00000321345.5:p.Glu569Ter
|
|
ENST00000637002.1:c.1096G>T
|
ENSP00000490340.1:p.Glu366Ter
|
|
ENST00000347310.9:c.1705G>T
|
ENSP00000321345.5:p.Glu569Ter
|
|
ENST00000395227.2:c.499G>T
|
ENSP00000378652.2:p.Glu167Ter
|
|
ENST00000425614.3:c.940G>T
|
ENSP00000387640.2:p.Glu314Ter
|
|
ENST00000473881.2:c.*531G>T
|
ENSP00000486667.1:n.*531G>T
|
|
NM_144701.2:c.1705G>T
|
NP_653302.2:p.Glu569Ter
|
|
XM_005270516.2:c.943G>T
|
XP_005270573.1:p.Glu315Ter
|
|
XM_011540789.1:c.1795G>T
|
XP_011539091.1:p.Glu599Ter
|
|
XM_011540790.1:c.1705G>T
|
XP_011539092.1:p.Glu569Ter
|
|
XM_011540791.1:c.1705G>T
|
XP_011539093.1:p.Glu569Ter
|
|
XM_011540790.3:c.1705G>T
|
XP_011539092.1:p.Glu569Ter
|
|
XM_011540791.3:c.1705G>T
|
XP_011539093.1:p.Glu569Ter
|
|
XR_001736993.1:n.1785G>T
|
|
|
NM_144701.3:c.1705G>T
MANE Select
|
NP_653302.2:p.Glu569Ter
|
|