ENST00000461574.2:c.5050A=
|
ENSP00000417241.2:p.Thr1684=
|
|
ENST00000470026.6:c.5053A=
|
ENSP00000419274.2:p.Thr1685=
|
|
ENST00000473961.6:c.4927A=
|
ENSP00000420201.2:p.Thr1643=
|
|
ENST00000476777.6:c.5047A=
|
ENSP00000417554.2:p.Thr1683=
|
|
ENST00000477152.6:c.4975A=
|
ENSP00000419988.2:p.Thr1659=
|
|
ENST00000478531.6:c.1741A=
|
ENSP00000420412.2:p.Thr581=
|
|
ENST00000489037.2:c.4975A=
|
ENSP00000420781.2:p.Thr1659=
|
|
ENST00000493919.6:c.1603A=
|
ENSP00000418819.2:p.Thr535=
|
|
ENST00000494123.6:c.5053A=
|
ENSP00000419103.2:p.Thr1685=
|
|
ENST00000497488.2:c.4165A=
|
ENSP00000418986.2:p.Thr1389=
|
|
ENST00000618469.2:c.5053A=
|
ENSP00000478114.2:p.Thr1685=
|
|
ENST00000634433.2:c.4930A=
|
ENSP00000489431.2:p.Thr1644=
|
|
ENST00000644379.2:c.5119A=
|
ENSP00000496570.2:p.Thr1707=
|
|
ENST00000644555.2:c.1603A=
|
ENSP00000494614.2:p.Thr535=
|
|
ENST00000652672.2:c.4912A=
|
ENSP00000498906.2:p.Thr1638=
|
|
ENST00000484087.6:c.1615A=
|
ENSP00000419481.2:p.Thr539=
|
|
ENST00000357654.9:c.5053A=
MANE Select
|
ENSP00000350283.3:p.Thr1685=
|
|
ENST00000471181.7:c.5116A=
|
ENSP00000418960.2:p.Thr1706=
|
|
ENST00000644379.1:c.1440A=
|
|
|
ENST00000352993.7:c.1627A=
|
ENSP00000312236.5:p.Thr543=
|
|
ENST00000357654.7:c.5053A=
|
ENSP00000350283.3:p.Thr1685=
|
|
ENST00000461221.5:c.*4836A=
|
ENSP00000418548.1:n.*4836A=
|
|
ENST00000468300.5:c.1741A=
|
ENSP00000417148.1:p.Thr581=
|
|
ENST00000471181.6:c.5116A=
|
ENSP00000418960.2:p.Thr1706=
|
|
ENST00000472490.1:n.206A=
|
|
|
ENST00000478531.5:c.1741A=
|
ENSP00000420412.1:p.Thr581=
|
|
ENST00000484087.5:c.1366A=
|
ENSP00000419481.1:p.Thr456=
|
|
ENST00000491747.6:c.1741A=
|
ENSP00000420705.2:p.Thr581=
|
|
ENST00000493795.5:c.4912A=
|
ENSP00000418775.1:p.Thr1638=
|
|
ENST00000493919.5:c.1603A=
|
ENSP00000418819.1:p.Thr535=
|
|
ENST00000586385.5:c.5-3678A=
|
ENSP00000465818.1:n.5-3678A=
|
|
ENST00000591534.5:c.526A=
|
ENSP00000467329.1:p.Thr176=
|
|
ENST00000591849.5:c.-98-17439A=
|
ENSP00000465347.1:n.-98-17439A=
|
|
NM_007294.3:c.5053A= , LRG_292t1:c.5053A=
|
NP_009225.1:p.Thr1685=
|
|
NM_007297.3:c.4912A=
|
NP_009228.2:p.Thr1638=
|
|
NM_007298.3:c.1741A=
|
NP_009229.2:p.Thr581=
|
|
NM_007299.3:c.1741A=
|
NP_009230.2:p.Thr581=
|
|
NM_007300.3:c.5116A=
|
NP_009231.2:p.Thr1706=
|
|
NR_027676.1:n.5189A=
|
|
|
NM_007294.4:c.5053A=
MANE Select
|
NP_009225.1:p.Thr1685=
|
|
NM_007297.4:c.4912A=
|
NP_009228.2:p.Thr1638=
|
|
NM_007299.4:c.1741A=
|
NP_009230.2:p.Thr581=
|
|
NM_007300.4:c.5116A=
|
NP_009231.2:p.Thr1706=
|
|
NR_027676.2:n.5230A=
|
|
|