ENST00000697149.1:c.1620T>A
|
ENSP00000513138.1:n.1620T>A
|
|
ENST00000697150.1:c.1678T>A
|
ENSP00000513139.1:n.1678T>A
|
|
ENST00000697151.1:c.1611T>A
|
ENSP00000513140.1:n.1611T>A
|
|
ENST00000697164.1:c.1691T>A
|
ENSP00000513153.1:p.Phe564Tyr
|
|
ENST00000697165.1:c.1478T>A
|
ENSP00000513154.1:p.Phe493Tyr
|
|
ENST00000347310.10:c.1781T>A
MANE Select
|
ENSP00000321345.5:p.Phe594Tyr
|
|
ENST00000637002.1:c.1172T>A
|
ENSP00000490340.1:p.Phe391Tyr
|
|
ENST00000347310.9:c.1781T>A
|
ENSP00000321345.5:p.Phe594Tyr
|
|
ENST00000395227.2:c.575T>A
|
ENSP00000378652.2:p.Phe192Tyr
|
|
ENST00000425614.3:c.1016T>A
|
ENSP00000387640.2:p.Phe339Tyr
|
|
ENST00000473881.2:c.*607T>A
|
ENSP00000486667.1:n.*607T>A
|
|
NM_144701.2:c.1781T>A
|
NP_653302.2:p.Phe594Tyr
|
|
XM_005270516.2:c.1019T>A
|
XP_005270573.1:p.Phe340Tyr
|
|
XM_011540789.1:c.1871T>A
|
XP_011539091.1:p.Phe624Tyr
|
|
XM_011540790.1:c.1781T>A
|
XP_011539092.1:p.Phe594Tyr
|
|
XM_011540791.1:c.1781T>A
|
XP_011539093.1:p.Phe594Tyr
|
|
XM_011540790.3:c.1781T>A
|
XP_011539092.1:p.Phe594Tyr
|
|
XM_011540791.3:c.1781T>A
|
XP_011539093.1:p.Phe594Tyr
|
|
XR_001736993.1:n.1861T>A
|
|
|
NM_144701.3:c.1781T>A
MANE Select
|
NP_653302.2:p.Phe594Tyr
|
|