ENST00000697149.1:c.1633G>T
|
ENSP00000513138.1:n.1633G>T
|
|
ENST00000697150.1:c.1691G>T
|
ENSP00000513139.1:n.1691G>T
|
|
ENST00000697151.1:c.1624G>T
|
ENSP00000513140.1:n.1624G>T
|
|
ENST00000697164.1:c.1704G>T
|
ENSP00000513153.1:p.Leu568Phe
|
|
ENST00000697165.1:c.1491G>T
|
ENSP00000513154.1:p.Leu497Phe
|
|
ENST00000347310.10:c.1794G>T
MANE Select
|
ENSP00000321345.5:p.Leu598Phe
|
|
ENST00000637002.1:c.1185G>T
|
ENSP00000490340.1:p.Leu395Phe
|
|
ENST00000347310.9:c.1794G>T
|
ENSP00000321345.5:p.Leu598Phe
|
|
ENST00000395227.2:c.588G>T
|
ENSP00000378652.2:p.Leu196Phe
|
|
ENST00000425614.3:c.1029G>T
|
ENSP00000387640.2:p.Leu343Phe
|
|
ENST00000473881.2:c.*620G>T
|
ENSP00000486667.1:n.*620G>T
|
|
NM_144701.2:c.1794G>T
|
NP_653302.2:p.Leu598Phe
|
|
XM_005270516.2:c.1032G>T
|
XP_005270573.1:p.Leu344Phe
|
|
XM_011540789.1:c.1884G>T
|
XP_011539091.1:p.Leu628Phe
|
|
XM_011540790.1:c.1794G>T
|
XP_011539092.1:p.Leu598Phe
|
|
XM_011540791.1:c.1794G>T
|
XP_011539093.1:p.Leu598Phe
|
|
XM_011540790.3:c.1794G>T
|
XP_011539092.1:p.Leu598Phe
|
|
XM_011540791.3:c.1794G>T
|
XP_011539093.1:p.Leu598Phe
|
|
XR_001736993.1:n.1874G>T
|
|
|
NM_144701.3:c.1794G>T
MANE Select
|
NP_653302.2:p.Leu598Phe
|
|