ENST00000697149.1:c.1331C>T
|
ENSP00000513138.1:n.1331C>T
|
|
ENST00000697150.1:c.1389C>T
|
ENSP00000513139.1:n.1389C>T
|
|
ENST00000697151.1:c.1322C>T
|
ENSP00000513140.1:n.1322C>T
|
|
ENST00000697164.1:c.1402C>T
|
ENSP00000513153.1:p.Leu468Phe
|
|
ENST00000697165.1:c.1189C>T
|
ENSP00000513154.1:p.Leu397Phe
|
|
ENST00000347310.10:c.1492C>T
MANE Select
|
ENSP00000321345.5:p.Leu498Phe
|
|
ENST00000637002.1:c.883C>T
|
ENSP00000490340.1:p.Leu295Phe
|
|
ENST00000347310.9:c.1492C>T
|
ENSP00000321345.5:p.Leu498Phe
|
|
ENST00000395227.2:c.286C>T
|
ENSP00000378652.2:p.Leu96Phe
|
|
ENST00000425614.3:c.727C>T
|
ENSP00000387640.2:p.Leu243Phe
|
|
ENST00000473881.2:c.*318C>T
|
ENSP00000486667.1:n.*318C>T
|
|
NM_144701.2:c.1492C>T
|
NP_653302.2:p.Leu498Phe
|
|
XM_005270516.2:c.730C>T
|
XP_005270573.1:p.Leu244Phe
|
|
XM_011540789.1:c.1582C>T
|
XP_011539091.1:p.Leu528Phe
|
|
XM_011540790.1:c.1492C>T
|
XP_011539092.1:p.Leu498Phe
|
|
XM_011540791.1:c.1492C>T
|
XP_011539093.1:p.Leu498Phe
|
|
XM_011540790.3:c.1492C>T
|
XP_011539092.1:p.Leu498Phe
|
|
XM_011540791.3:c.1492C>T
|
XP_011539093.1:p.Leu498Phe
|
|
XR_001736993.1:n.1572C>T
|
|
|
NM_144701.3:c.1492C>T
MANE Select
|
NP_653302.2:p.Leu498Phe
|
|