ENST00000697149.1:c.1366T>G
|
ENSP00000513138.1:n.1366T>G
|
|
ENST00000697150.1:c.1424T>G
|
ENSP00000513139.1:n.1424T>G
|
|
ENST00000697151.1:c.1357T>G
|
ENSP00000513140.1:n.1357T>G
|
|
ENST00000697164.1:c.1437T>G
|
ENSP00000513153.1:p.Leu479=
|
|
ENST00000697165.1:c.1224T>G
|
ENSP00000513154.1:p.Leu408=
|
|
ENST00000347310.10:c.1527T>G
MANE Select
|
ENSP00000321345.5:p.Leu509=
|
|
ENST00000637002.1:c.918T>G
|
ENSP00000490340.1:p.Leu306=
|
|
ENST00000347310.9:c.1527T>G
|
ENSP00000321345.5:p.Leu509=
|
|
ENST00000395227.2:c.321T>G
|
ENSP00000378652.2:p.Leu107=
|
|
ENST00000425614.3:c.762T>G
|
ENSP00000387640.2:p.Leu254=
|
|
ENST00000473881.2:c.*353T>G
|
ENSP00000486667.1:n.*353T>G
|
|
NM_144701.2:c.1527T>G
|
NP_653302.2:p.Leu509=
|
|
XM_005270516.2:c.765T>G
|
XP_005270573.1:p.Leu255=
|
|
XM_011540789.1:c.1617T>G
|
XP_011539091.1:p.Leu539=
|
|
XM_011540790.1:c.1527T>G
|
XP_011539092.1:p.Leu509=
|
|
XM_011540791.1:c.1527T>G
|
XP_011539093.1:p.Leu509=
|
|
XM_011540790.3:c.1527T>G
|
XP_011539092.1:p.Leu509=
|
|
XM_011540791.3:c.1527T>G
|
XP_011539093.1:p.Leu509=
|
|
XR_001736993.1:n.1607T>G
|
|
|
NM_144701.3:c.1527T>G
MANE Select
|
NP_653302.2:p.Leu509=
|
|