ENST00000461574.2:c.5049T>A
|
ENSP00000417241.2:p.Thr1683=
|
|
ENST00000470026.6:c.5052T>A
|
ENSP00000419274.2:p.Thr1684=
|
|
ENST00000473961.6:c.4926T>A
|
ENSP00000420201.2:p.Thr1642=
|
|
ENST00000476777.6:c.5046T>A
|
ENSP00000417554.2:p.Thr1682=
|
|
ENST00000477152.6:c.4974T>A
|
ENSP00000419988.2:p.Thr1658=
|
|
ENST00000478531.6:c.1740T>A
|
ENSP00000420412.2:p.Thr580=
|
|
ENST00000489037.2:c.4974T>A
|
ENSP00000420781.2:p.Thr1658=
|
|
ENST00000493919.6:c.1602T>A
|
ENSP00000418819.2:p.Thr534=
|
|
ENST00000494123.6:c.5052T>A
|
ENSP00000419103.2:p.Thr1684=
|
|
ENST00000497488.2:c.4164T>A
|
ENSP00000418986.2:p.Thr1388=
|
|
ENST00000618469.2:c.5052T>A
|
ENSP00000478114.2:p.Thr1684=
|
|
ENST00000634433.2:c.4929T>A
|
ENSP00000489431.2:p.Thr1643=
|
|
ENST00000644379.2:c.5118T>A
|
ENSP00000496570.2:p.Thr1706=
|
|
ENST00000644555.2:c.1602T>A
|
ENSP00000494614.2:p.Thr534=
|
|
ENST00000652672.2:c.4911T>A
|
ENSP00000498906.2:p.Thr1637=
|
|
ENST00000484087.6:c.1614T>A
|
ENSP00000419481.2:p.Thr538=
|
|
ENST00000357654.9:c.5052T>A
MANE Select
|
ENSP00000350283.3:p.Thr1684=
|
|
ENST00000471181.7:c.5115T>A
|
ENSP00000418960.2:p.Thr1705=
|
|
ENST00000644379.1:c.1439T>A
|
|
|
ENST00000352993.7:c.1626T>A
|
ENSP00000312236.5:p.Thr542=
|
|
ENST00000357654.7:c.5052T>A
|
ENSP00000350283.3:p.Thr1684=
|
|
ENST00000461221.5:c.*4835T>A
|
ENSP00000418548.1:n.*4835T>A
|
|
ENST00000468300.5:c.1740T>A
|
ENSP00000417148.1:p.Thr580=
|
|
ENST00000471181.6:c.5115T>A
|
ENSP00000418960.2:p.Thr1705=
|
|
ENST00000472490.1:n.205T>A
|
|
|
ENST00000478531.5:c.1740T>A
|
ENSP00000420412.1:p.Thr580=
|
|
ENST00000484087.5:c.1365T>A
|
ENSP00000419481.1:p.Thr455=
|
|
ENST00000491747.6:c.1740T>A
|
ENSP00000420705.2:p.Thr580=
|
|
ENST00000493795.5:c.4911T>A
|
ENSP00000418775.1:p.Thr1637=
|
|
ENST00000493919.5:c.1602T>A
|
ENSP00000418819.1:p.Thr534=
|
|
ENST00000586385.5:c.5-3679T>A
|
ENSP00000465818.1:n.5-3679T>A
|
|
ENST00000591534.5:c.525T>A
|
ENSP00000467329.1:p.Thr175=
|
|
ENST00000591849.5:c.-98-17440T>A
|
ENSP00000465347.1:n.-98-17440T>A
|
|
NM_007294.3:c.5052T>A , LRG_292t1:c.5052T>A
|
NP_009225.1:p.Thr1684=
|
|
NM_007297.3:c.4911T>A
|
NP_009228.2:p.Thr1637=
|
|
NM_007298.3:c.1740T>A
|
NP_009229.2:p.Thr580=
|
|
NM_007299.3:c.1740T>A
|
NP_009230.2:p.Thr580=
|
|
NM_007300.3:c.5115T>A
|
NP_009231.2:p.Thr1705=
|
|
NR_027676.1:n.5188T>A
|
|
|
NM_007294.4:c.5052T>A
MANE Select
|
NP_009225.1:p.Thr1684=
|
|
NM_007297.4:c.4911T>A
|
NP_009228.2:p.Thr1637=
|
|
NM_007299.4:c.1740T>A
|
NP_009230.2:p.Thr580=
|
|
NM_007300.4:c.5115T>A
|
NP_009231.2:p.Thr1705=
|
|
NR_027676.2:n.5229T>A
|
|
|