ENST00000697149.1:c.1354T>A
|
ENSP00000513138.1:n.1354T>A
|
|
ENST00000697150.1:c.1412T>A
|
ENSP00000513139.1:n.1412T>A
|
|
ENST00000697151.1:c.1345T>A
|
ENSP00000513140.1:n.1345T>A
|
|
ENST00000697164.1:c.1425T>A
|
ENSP00000513153.1:p.Thr475=
|
|
ENST00000697165.1:c.1212T>A
|
ENSP00000513154.1:p.Thr404=
|
|
ENST00000347310.10:c.1515T>A
MANE Select
|
ENSP00000321345.5:p.Thr505=
|
|
ENST00000637002.1:c.906T>A
|
ENSP00000490340.1:p.Thr302=
|
|
ENST00000347310.9:c.1515T>A
|
ENSP00000321345.5:p.Thr505=
|
|
ENST00000395227.2:c.309T>A
|
ENSP00000378652.2:p.Thr103=
|
|
ENST00000425614.3:c.750T>A
|
ENSP00000387640.2:p.Thr250=
|
|
ENST00000473881.2:c.*341T>A
|
ENSP00000486667.1:n.*341T>A
|
|
NM_144701.2:c.1515T>A
|
NP_653302.2:p.Thr505=
|
|
XM_005270516.2:c.753T>A
|
XP_005270573.1:p.Thr251=
|
|
XM_011540789.1:c.1605T>A
|
XP_011539091.1:p.Thr535=
|
|
XM_011540790.1:c.1515T>A
|
XP_011539092.1:p.Thr505=
|
|
XM_011540791.1:c.1515T>A
|
XP_011539093.1:p.Thr505=
|
|
XM_011540790.3:c.1515T>A
|
XP_011539092.1:p.Thr505=
|
|
XM_011540791.3:c.1515T>A
|
XP_011539093.1:p.Thr505=
|
|
XR_001736993.1:n.1595T>A
|
|
|
NM_144701.3:c.1515T>A
MANE Select
|
NP_653302.2:p.Thr505=
|
|