ENST00000461574.2:c.5289A>T
|
ENSP00000417241.2:p.Leu1763=
|
|
ENST00000470026.6:c.5292A>T
|
ENSP00000419274.2:p.Leu1764=
|
|
ENST00000473961.6:c.5166A>T
|
ENSP00000420201.2:p.Leu1722=
|
|
ENST00000476777.6:c.5286A>T
|
ENSP00000417554.2:p.Leu1762=
|
|
ENST00000477152.6:c.5214A>T
|
ENSP00000419988.2:p.Leu1738=
|
|
ENST00000478531.6:c.1980A>T
|
ENSP00000420412.2:p.Leu660=
|
|
ENST00000489037.2:c.5214A>T
|
ENSP00000420781.2:p.Leu1738=
|
|
ENST00000493919.6:c.1842A>T
|
ENSP00000418819.2:p.Leu614=
|
|
ENST00000494123.6:c.5292A>T
|
ENSP00000419103.2:p.Leu1764=
|
|
ENST00000497488.2:c.4404A>T
|
ENSP00000418986.2:p.Leu1468=
|
|
ENST00000618469.2:c.5292A>T
|
ENSP00000478114.2:p.Leu1764=
|
|
ENST00000634433.2:c.5169A>T
|
ENSP00000489431.2:p.Leu1723=
|
|
ENST00000644379.2:c.5358A>T
|
ENSP00000496570.2:p.Leu1786=
|
|
ENST00000644555.2:c.1842A>T
|
ENSP00000494614.2:p.Leu614=
|
|
ENST00000652672.2:c.5151A>T
|
ENSP00000498906.2:p.Leu1717=
|
|
ENST00000484087.6:c.1854A>T
|
ENSP00000419481.2:p.Leu618=
|
|
ENST00000357654.9:c.5292A>T
MANE Select
|
ENSP00000350283.3:p.Leu1764=
|
|
ENST00000471181.7:c.5355A>T
|
ENSP00000418960.2:p.Leu1785=
|
|
ENST00000644379.1:c.1679A>T
|
|
|
ENST00000352993.7:c.1866A>T
|
ENSP00000312236.5:p.Leu622=
|
|
ENST00000357654.7:c.5292A>T
|
ENSP00000350283.3:p.Leu1764=
|
|
ENST00000461221.5:c.*5075A>T
|
ENSP00000418548.1:n.*5075A>T
|
|
ENST00000468300.5:c.1980A>T
|
ENSP00000417148.1:p.Leu660=
|
|
ENST00000471181.6:c.5355A>T
|
ENSP00000418960.2:p.Leu1785=
|
|
ENST00000491747.6:c.1980A>T
|
ENSP00000420705.2:p.Leu660=
|
|
ENST00000493795.5:c.5151A>T
|
ENSP00000418775.1:p.Leu1717=
|
|
ENST00000586385.5:c.222A>T
|
ENSP00000465818.1:p.Leu74=
|
|
ENST00000591534.5:c.765A>T
|
ENSP00000467329.1:p.Leu255=
|
|
ENST00000591849.5:c.-98-913A>T
|
ENSP00000465347.1:n.-98-913A>T
|
|
NM_007294.3:c.5292A>T , LRG_292t1:c.5292A>T
|
NP_009225.1:p.Leu1764=
|
|
NM_007297.3:c.5151A>T
|
NP_009228.2:p.Leu1717=
|
|
NM_007298.3:c.1980A>T
|
NP_009229.2:p.Leu660=
|
|
NM_007299.3:c.1980A>T
|
NP_009230.2:p.Leu660=
|
|
NM_007300.3:c.5355A>T
|
NP_009231.2:p.Leu1785=
|
|
NR_027676.1:n.5428A>T
|
|
|
NM_007294.4:c.5292A>T
MANE Select
|
NP_009225.1:p.Leu1764=
|
|
NM_007297.4:c.5151A>T
|
NP_009228.2:p.Leu1717=
|
|
NM_007299.4:c.1980A>T
|
NP_009230.2:p.Leu660=
|
|
NM_007300.4:c.5355A>T
|
NP_009231.2:p.Leu1785=
|
|
NR_027676.2:n.5469A>T
|
|
|