ENST00000461574.2:c.4854T>G
|
ENSP00000417241.2:p.Thr1618=
|
|
ENST00000470026.6:c.4857T>G
|
ENSP00000419274.2:p.Thr1619=
|
|
ENST00000473961.6:c.4731T>G
|
ENSP00000420201.2:p.Thr1577=
|
|
ENST00000476777.6:c.4851T>G
|
ENSP00000417554.2:p.Thr1617=
|
|
ENST00000477152.6:c.4779T>G
|
ENSP00000419988.2:p.Thr1593=
|
|
ENST00000478531.6:c.1545T>G
|
ENSP00000420412.2:p.Thr515=
|
|
ENST00000489037.2:c.4779T>G
|
ENSP00000420781.2:p.Thr1593=
|
|
ENST00000493919.6:c.1407T>G
|
ENSP00000418819.2:p.Thr469=
|
|
ENST00000494123.6:c.4857T>G
|
ENSP00000419103.2:p.Thr1619=
|
|
ENST00000497488.2:c.3969T>G
|
ENSP00000418986.2:p.Thr1323=
|
|
ENST00000618469.2:c.4857T>G
|
ENSP00000478114.2:p.Thr1619=
|
|
ENST00000634433.2:c.4734T>G
|
ENSP00000489431.2:p.Thr1578=
|
|
ENST00000644379.2:c.4923T>G
|
ENSP00000496570.2:p.Thr1641=
|
|
ENST00000644555.2:c.1407T>G
|
ENSP00000494614.2:p.Thr469=
|
|
ENST00000652672.2:c.4716T>G
|
ENSP00000498906.2:p.Thr1572=
|
|
ENST00000484087.6:c.1419T>G
|
ENSP00000419481.2:p.Thr473=
|
|
ENST00000700182.1:c.1464T>G
|
ENSP00000514849.1:p.Thr488=
|
|
ENST00000357654.9:c.4857T>G
MANE Select
|
ENSP00000350283.3:p.Thr1619=
|
|
ENST00000471181.7:c.4920T>G
|
ENSP00000418960.2:p.Thr1640=
|
|
ENST00000644379.1:c.1244T>G
|
|
|
ENST00000352993.7:c.1431T>G
|
ENSP00000312236.5:p.Thr477=
|
|
ENST00000357654.7:c.4857T>G
|
ENSP00000350283.3:p.Thr1619=
|
|
ENST00000461221.5:c.*4640T>G
|
ENSP00000418548.1:n.*4640T>G
|
|
ENST00000468300.5:c.1545T>G
|
ENSP00000417148.1:p.Thr515=
|
|
ENST00000471181.6:c.4920T>G
|
ENSP00000418960.2:p.Thr1640=
|
|
ENST00000472490.1:n.10T>G
|
|
|
ENST00000478531.5:c.1545T>G
|
ENSP00000420412.1:p.Thr515=
|
|
ENST00000484087.5:c.1170T>G
|
ENSP00000419481.1:p.Thr390=
|
|
ENST00000491747.6:c.1545T>G
|
ENSP00000420705.2:p.Thr515=
|
|
ENST00000493795.5:c.4716T>G
|
ENSP00000418775.1:p.Thr1572=
|
|
ENST00000493919.5:c.1407T>G
|
ENSP00000418819.1:p.Thr469=
|
|
ENST00000586385.5:c.5-7106T>G
|
ENSP00000465818.1:n.5-7106T>G
|
|
ENST00000591534.5:c.330T>G
|
ENSP00000467329.1:p.Thr110=
|
|
ENST00000591849.5:c.-98-20867T>G
|
ENSP00000465347.1:n.-98-20867T>G
|
|
NM_007294.3:c.4857T>G , LRG_292t1:c.4857T>G
|
NP_009225.1:p.Thr1619=
|
|
NM_007297.3:c.4716T>G
|
NP_009228.2:p.Thr1572=
|
|
NM_007298.3:c.1545T>G
|
NP_009229.2:p.Thr515=
|
|
NM_007299.3:c.1545T>G
|
NP_009230.2:p.Thr515=
|
|
NM_007300.3:c.4920T>G
|
NP_009231.2:p.Thr1640=
|
|
NR_027676.1:n.4993T>G
|
|
|
NM_007294.4:c.4857T>G
MANE Select
|
NP_009225.1:p.Thr1619=
|
|
NM_007297.4:c.4716T>G
|
NP_009228.2:p.Thr1572=
|
|
NM_007299.4:c.1545T>G
|
NP_009230.2:p.Thr515=
|
|
NM_007300.4:c.4920T>G
|
NP_009231.2:p.Thr1640=
|
|
NR_027676.2:n.5034T>G
|
|
|