ENST00000697149.1:c.1598C>A
|
ENSP00000513138.1:n.1598C>A
|
|
ENST00000697150.1:c.1656C>A
|
ENSP00000513139.1:n.1656C>A
|
|
ENST00000697151.1:c.1589C>A
|
ENSP00000513140.1:n.1589C>A
|
|
ENST00000697164.1:c.1669C>A
|
ENSP00000513153.1:p.Gln557Lys
|
|
ENST00000697165.1:c.1456C>A
|
ENSP00000513154.1:p.Gln486Lys
|
|
ENST00000347310.10:c.1759C>A
MANE Select
|
ENSP00000321345.5:p.Gln587Lys
|
|
ENST00000637002.1:c.1150C>A
|
ENSP00000490340.1:p.Gln384Lys
|
|
ENST00000347310.9:c.1759C>A
|
ENSP00000321345.5:p.Gln587Lys
|
|
ENST00000395227.2:c.553C>A
|
ENSP00000378652.2:p.Gln185Lys
|
|
ENST00000425614.3:c.994C>A
|
ENSP00000387640.2:p.Gln332Lys
|
|
ENST00000473881.2:c.*585C>A
|
ENSP00000486667.1:n.*585C>A
|
|
NM_144701.2:c.1759C>A
|
NP_653302.2:p.Gln587Lys
|
|
XM_005270516.2:c.997C>A
|
XP_005270573.1:p.Gln333Lys
|
|
XM_011540789.1:c.1849C>A
|
XP_011539091.1:p.Gln617Lys
|
|
XM_011540790.1:c.1759C>A
|
XP_011539092.1:p.Gln587Lys
|
|
XM_011540791.1:c.1759C>A
|
XP_011539093.1:p.Gln587Lys
|
|
XM_011540790.3:c.1759C>A
|
XP_011539092.1:p.Gln587Lys
|
|
XM_011540791.3:c.1759C>A
|
XP_011539093.1:p.Gln587Lys
|
|
XR_001736993.1:n.1839C>A
|
|
|
NM_144701.3:c.1759C>A
MANE Select
|
NP_653302.2:p.Gln587Lys
|
|