ENST00000697149.1:c.1508G>T
|
ENSP00000513138.1:n.1508G>T
|
|
ENST00000697150.1:c.1566G>T
|
ENSP00000513139.1:n.1566G>T
|
|
ENST00000697151.1:c.1499G>T
|
ENSP00000513140.1:n.1499G>T
|
|
ENST00000697164.1:c.1579G>T
|
ENSP00000513153.1:p.Glu527Ter
|
|
ENST00000697165.1:c.1366G>T
|
ENSP00000513154.1:p.Glu456Ter
|
|
ENST00000347310.10:c.1669G>T
MANE Select
|
ENSP00000321345.5:p.Glu557Ter
|
|
ENST00000637002.1:c.1060G>T
|
ENSP00000490340.1:p.Glu354Ter
|
|
ENST00000347310.9:c.1669G>T
|
ENSP00000321345.5:p.Glu557Ter
|
|
ENST00000395227.2:c.463G>T
|
ENSP00000378652.2:p.Glu155Ter
|
|
ENST00000425614.3:c.904G>T
|
ENSP00000387640.2:p.Glu302Ter
|
|
ENST00000473881.2:c.*495G>T
|
ENSP00000486667.1:n.*495G>T
|
|
NM_144701.2:c.1669G>T
|
NP_653302.2:p.Glu557Ter
|
|
XM_005270516.2:c.907G>T
|
XP_005270573.1:p.Glu303Ter
|
|
XM_011540789.1:c.1759G>T
|
XP_011539091.1:p.Glu587Ter
|
|
XM_011540790.1:c.1669G>T
|
XP_011539092.1:p.Glu557Ter
|
|
XM_011540791.1:c.1669G>T
|
XP_011539093.1:p.Glu557Ter
|
|
XM_011540790.3:c.1669G>T
|
XP_011539092.1:p.Glu557Ter
|
|
XM_011540791.3:c.1669G>T
|
XP_011539093.1:p.Glu557Ter
|
|
XR_001736993.1:n.1749G>T
|
|
|
NM_144701.3:c.1669G>T
MANE Select
|
NP_653302.2:p.Glu557Ter
|
|