ENST00000461574.2:c.5271A>G
|
ENSP00000417241.2:p.Arg1757=
|
|
ENST00000470026.6:c.5274A>G
|
ENSP00000419274.2:p.Arg1758=
|
|
ENST00000473961.6:c.5148A>G
|
ENSP00000420201.2:p.Arg1716=
|
|
ENST00000476777.6:c.5268A>G
|
ENSP00000417554.2:p.Arg1756=
|
|
ENST00000477152.6:c.5196A>G
|
ENSP00000419988.2:p.Arg1732=
|
|
ENST00000478531.6:c.1962A>G
|
ENSP00000420412.2:p.Arg654=
|
|
ENST00000489037.2:c.5196A>G
|
ENSP00000420781.2:p.Arg1732=
|
|
ENST00000493919.6:c.1824A>G
|
ENSP00000418819.2:p.Arg608=
|
|
ENST00000494123.6:c.5274A>G
|
ENSP00000419103.2:p.Arg1758=
|
|
ENST00000497488.2:c.4386A>G
|
ENSP00000418986.2:p.Arg1462=
|
|
ENST00000618469.2:c.5274A>G
|
ENSP00000478114.2:p.Arg1758=
|
|
ENST00000634433.2:c.5151A>G
|
ENSP00000489431.2:p.Arg1717=
|
|
ENST00000644379.2:c.5340A>G
|
ENSP00000496570.2:p.Arg1780=
|
|
ENST00000644555.2:c.1824A>G
|
ENSP00000494614.2:p.Arg608=
|
|
ENST00000652672.2:c.5133A>G
|
ENSP00000498906.2:p.Arg1711=
|
|
ENST00000484087.6:c.1836A>G
|
ENSP00000419481.2:p.Arg612=
|
|
ENST00000357654.9:c.5274A>G
MANE Select
|
ENSP00000350283.3:p.Arg1758=
|
|
ENST00000471181.7:c.5337A>G
|
ENSP00000418960.2:p.Arg1779=
|
|
ENST00000644379.1:c.1661A>G
|
|
|
ENST00000352993.7:c.1848A>G
|
ENSP00000312236.5:p.Arg616=
|
|
ENST00000357654.7:c.5274A>G
|
ENSP00000350283.3:p.Arg1758=
|
|
ENST00000461221.5:c.*5057A>G
|
ENSP00000418548.1:n.*5057A>G
|
|
ENST00000468300.5:c.1962A>G
|
ENSP00000417148.1:p.Arg654=
|
|
ENST00000471181.6:c.5337A>G
|
ENSP00000418960.2:p.Arg1779=
|
|
ENST00000491747.6:c.1962A>G
|
ENSP00000420705.2:p.Arg654=
|
|
ENST00000493795.5:c.5133A>G
|
ENSP00000418775.1:p.Arg1711=
|
|
ENST00000586385.5:c.204A>G
|
ENSP00000465818.1:p.Arg68=
|
|
ENST00000591534.5:c.747A>G
|
ENSP00000467329.1:p.Arg249=
|
|
ENST00000591849.5:c.-98-6865A>G
|
ENSP00000465347.1:n.-98-6865A>G
|
|
NM_007294.3:c.5274A>G , LRG_292t1:c.5274A>G
|
NP_009225.1:p.Arg1758=
|
|
NM_007297.3:c.5133A>G
|
NP_009228.2:p.Arg1711=
|
|
NM_007298.3:c.1962A>G
|
NP_009229.2:p.Arg654=
|
|
NM_007299.3:c.1962A>G
|
NP_009230.2:p.Arg654=
|
|
NM_007300.3:c.5337A>G
|
NP_009231.2:p.Arg1779=
|
|
NR_027676.1:n.5410A>G
|
|
|
NM_007294.4:c.5274A>G
MANE Select
|
NP_009225.1:p.Arg1758=
|
|
NM_007297.4:c.5133A>G
|
NP_009228.2:p.Arg1711=
|
|
NM_007299.4:c.1962A>G
|
NP_009230.2:p.Arg654=
|
|
NM_007300.4:c.5337A>G
|
NP_009231.2:p.Arg1779=
|
|
NR_027676.2:n.5451A>G
|
|
|