ENST00000697149.1:c.1404C>A
|
ENSP00000513138.1:n.1404C>A
|
|
ENST00000697150.1:c.1462C>A
|
ENSP00000513139.1:n.1462C>A
|
|
ENST00000697151.1:c.1395C>A
|
ENSP00000513140.1:n.1395C>A
|
|
ENST00000697164.1:c.1475C>A
|
ENSP00000513153.1:p.Pro492His
|
|
ENST00000697165.1:c.1262C>A
|
ENSP00000513154.1:p.Pro421His
|
|
ENST00000347310.10:c.1565C>A
MANE Select
|
ENSP00000321345.5:p.Pro522His
|
|
ENST00000637002.1:c.956C>A
|
ENSP00000490340.1:p.Pro319His
|
|
ENST00000347310.9:c.1565C>A
|
ENSP00000321345.5:p.Pro522His
|
|
ENST00000395227.2:c.359C>A
|
ENSP00000378652.2:p.Pro120His
|
|
ENST00000425614.3:c.800C>A
|
ENSP00000387640.2:p.Pro267His
|
|
ENST00000473881.2:c.*391C>A
|
ENSP00000486667.1:n.*391C>A
|
|
NM_144701.2:c.1565C>A
|
NP_653302.2:p.Pro522His
|
|
XM_005270516.2:c.803C>A
|
XP_005270573.1:p.Pro268His
|
|
XM_011540789.1:c.1655C>A
|
XP_011539091.1:p.Pro552His
|
|
XM_011540790.1:c.1565C>A
|
XP_011539092.1:p.Pro522His
|
|
XM_011540791.1:c.1565C>A
|
XP_011539093.1:p.Pro522His
|
|
XM_011540790.3:c.1565C>A
|
XP_011539092.1:p.Pro522His
|
|
XM_011540791.3:c.1565C>A
|
XP_011539093.1:p.Pro522His
|
|
XR_001736993.1:n.1645C>A
|
|
|
NM_144701.3:c.1565C>A
MANE Select
|
NP_653302.2:p.Pro522His
|
|