ENST00000697149.1:c.1421C>A
|
ENSP00000513138.1:n.1421C>A
|
|
ENST00000697150.1:c.1479C>A
|
ENSP00000513139.1:n.1479C>A
|
|
ENST00000697151.1:c.1412C>A
|
ENSP00000513140.1:n.1412C>A
|
|
ENST00000697164.1:c.1492C>A
|
ENSP00000513153.1:p.Pro498Thr
|
|
ENST00000697165.1:c.1279C>A
|
ENSP00000513154.1:p.Pro427Thr
|
|
ENST00000347310.10:c.1582C>A
MANE Select
|
ENSP00000321345.5:p.Pro528Thr
|
|
ENST00000637002.1:c.973C>A
|
ENSP00000490340.1:p.Pro325Thr
|
|
ENST00000347310.9:c.1582C>A
|
ENSP00000321345.5:p.Pro528Thr
|
|
ENST00000395227.2:c.376C>A
|
ENSP00000378652.2:p.Pro126Thr
|
|
ENST00000425614.3:c.817C>A
|
ENSP00000387640.2:p.Pro273Thr
|
|
ENST00000473881.2:c.*408C>A
|
ENSP00000486667.1:n.*408C>A
|
|
NM_144701.2:c.1582C>A
|
NP_653302.2:p.Pro528Thr
|
|
XM_005270516.2:c.820C>A
|
XP_005270573.1:p.Pro274Thr
|
|
XM_011540789.1:c.1672C>A
|
XP_011539091.1:p.Pro558Thr
|
|
XM_011540790.1:c.1582C>A
|
XP_011539092.1:p.Pro528Thr
|
|
XM_011540791.1:c.1582C>A
|
XP_011539093.1:p.Pro528Thr
|
|
XM_011540790.3:c.1582C>A
|
XP_011539092.1:p.Pro528Thr
|
|
XM_011540791.3:c.1582C>A
|
XP_011539093.1:p.Pro528Thr
|
|
XR_001736993.1:n.1662C>A
|
|
|
NM_144701.3:c.1582C>A
MANE Select
|
NP_653302.2:p.Pro528Thr
|
|