ENST00000697149.1:c.1352A>G
|
ENSP00000513138.1:n.1352A>G
|
|
ENST00000697150.1:c.1410A>G
|
ENSP00000513139.1:n.1410A>G
|
|
ENST00000697151.1:c.1343A>G
|
ENSP00000513140.1:n.1343A>G
|
|
ENST00000697164.1:c.1423A>G
|
ENSP00000513153.1:p.Thr475Ala
|
|
ENST00000697165.1:c.1210A>G
|
ENSP00000513154.1:p.Thr404Ala
|
|
ENST00000347310.10:c.1513A>G
MANE Select
|
ENSP00000321345.5:p.Thr505Ala
|
|
ENST00000637002.1:c.904A>G
|
ENSP00000490340.1:p.Thr302Ala
|
|
ENST00000347310.9:c.1513A>G
|
ENSP00000321345.5:p.Thr505Ala
|
|
ENST00000395227.2:c.307A>G
|
ENSP00000378652.2:p.Thr103Ala
|
|
ENST00000425614.3:c.748A>G
|
ENSP00000387640.2:p.Thr250Ala
|
|
ENST00000473881.2:c.*339A>G
|
ENSP00000486667.1:n.*339A>G
|
|
NM_144701.2:c.1513A>G
|
NP_653302.2:p.Thr505Ala
|
|
XM_005270516.2:c.751A>G
|
XP_005270573.1:p.Thr251Ala
|
|
XM_011540789.1:c.1603A>G
|
XP_011539091.1:p.Thr535Ala
|
|
XM_011540790.1:c.1513A>G
|
XP_011539092.1:p.Thr505Ala
|
|
XM_011540791.1:c.1513A>G
|
XP_011539093.1:p.Thr505Ala
|
|
XM_011540790.3:c.1513A>G
|
XP_011539092.1:p.Thr505Ala
|
|
XM_011540791.3:c.1513A>G
|
XP_011539093.1:p.Thr505Ala
|
|
XR_001736993.1:n.1593A>G
|
|
|
NM_144701.3:c.1513A>G
MANE Select
|
NP_653302.2:p.Thr505Ala
|
|