ENST00000697149.1:c.1350T>C
|
ENSP00000513138.1:n.1350T>C
|
|
ENST00000697150.1:c.1408T>C
|
ENSP00000513139.1:n.1408T>C
|
|
ENST00000697151.1:c.1341T>C
|
ENSP00000513140.1:n.1341T>C
|
|
ENST00000697164.1:c.1421T>C
|
ENSP00000513153.1:p.Ile474Thr
|
|
ENST00000697165.1:c.1208T>C
|
ENSP00000513154.1:p.Ile403Thr
|
|
ENST00000347310.10:c.1511T>C
MANE Select
|
ENSP00000321345.5:p.Ile504Thr
|
|
ENST00000637002.1:c.902T>C
|
ENSP00000490340.1:p.Ile301Thr
|
|
ENST00000347310.9:c.1511T>C
|
ENSP00000321345.5:p.Ile504Thr
|
|
ENST00000395227.2:c.305T>C
|
ENSP00000378652.2:p.Ile102Thr
|
|
ENST00000425614.3:c.746T>C
|
ENSP00000387640.2:p.Ile249Thr
|
|
ENST00000473881.2:c.*337T>C
|
ENSP00000486667.1:n.*337T>C
|
|
NM_144701.2:c.1511T>C
|
NP_653302.2:p.Ile504Thr
|
|
XM_005270516.2:c.749T>C
|
XP_005270573.1:p.Ile250Thr
|
|
XM_011540789.1:c.1601T>C
|
XP_011539091.1:p.Ile534Thr
|
|
XM_011540790.1:c.1511T>C
|
XP_011539092.1:p.Ile504Thr
|
|
XM_011540791.1:c.1511T>C
|
XP_011539093.1:p.Ile504Thr
|
|
XM_011540790.3:c.1511T>C
|
XP_011539092.1:p.Ile504Thr
|
|
XM_011540791.3:c.1511T>C
|
XP_011539093.1:p.Ile504Thr
|
|
XR_001736993.1:n.1591T>C
|
|
|
NM_144701.3:c.1511T>C
MANE Select
|
NP_653302.2:p.Ile504Thr
|
|