ENST00000697149.1:c.1353C>T
|
ENSP00000513138.1:n.1353C>T
|
|
ENST00000697150.1:c.1411C>T
|
ENSP00000513139.1:n.1411C>T
|
|
ENST00000697151.1:c.1344C>T
|
ENSP00000513140.1:n.1344C>T
|
|
ENST00000697164.1:c.1424C>T
|
ENSP00000513153.1:p.Thr475Ile
|
|
ENST00000697165.1:c.1211C>T
|
ENSP00000513154.1:p.Thr404Ile
|
|
ENST00000347310.10:c.1514C>T
MANE Select
|
ENSP00000321345.5:p.Thr505Ile
|
|
ENST00000637002.1:c.905C>T
|
ENSP00000490340.1:p.Thr302Ile
|
|
ENST00000347310.9:c.1514C>T
|
ENSP00000321345.5:p.Thr505Ile
|
|
ENST00000395227.2:c.308C>T
|
ENSP00000378652.2:p.Thr103Ile
|
|
ENST00000425614.3:c.749C>T
|
ENSP00000387640.2:p.Thr250Ile
|
|
ENST00000473881.2:c.*340C>T
|
ENSP00000486667.1:n.*340C>T
|
|
NM_144701.2:c.1514C>T
|
NP_653302.2:p.Thr505Ile
|
|
XM_005270516.2:c.752C>T
|
XP_005270573.1:p.Thr251Ile
|
|
XM_011540789.1:c.1604C>T
|
XP_011539091.1:p.Thr535Ile
|
|
XM_011540790.1:c.1514C>T
|
XP_011539092.1:p.Thr505Ile
|
|
XM_011540791.1:c.1514C>T
|
XP_011539093.1:p.Thr505Ile
|
|
XM_011540790.3:c.1514C>T
|
XP_011539092.1:p.Thr505Ile
|
|
XM_011540791.3:c.1514C>T
|
XP_011539093.1:p.Thr505Ile
|
|
XR_001736993.1:n.1594C>T
|
|
|
NM_144701.3:c.1514C>T
MANE Select
|
NP_653302.2:p.Thr505Ile
|
|