ENST00000461574.2:c.5040T=
|
ENSP00000417241.2:p.Thr1680=
|
|
ENST00000470026.6:c.5043T=
|
ENSP00000419274.2:p.Thr1681=
|
|
ENST00000473961.6:c.4917T=
|
ENSP00000420201.2:p.Thr1639=
|
|
ENST00000476777.6:c.5037T=
|
ENSP00000417554.2:p.Thr1679=
|
|
ENST00000477152.6:c.4965T=
|
ENSP00000419988.2:p.Thr1655=
|
|
ENST00000478531.6:c.1731T=
|
ENSP00000420412.2:p.Thr577=
|
|
ENST00000489037.2:c.4965T=
|
ENSP00000420781.2:p.Thr1655=
|
|
ENST00000493919.6:c.1593T=
|
ENSP00000418819.2:p.Thr531=
|
|
ENST00000494123.6:c.5043T=
|
ENSP00000419103.2:p.Thr1681=
|
|
ENST00000497488.2:c.4155T=
|
ENSP00000418986.2:p.Thr1385=
|
|
ENST00000618469.2:c.5043T=
|
ENSP00000478114.2:p.Thr1681=
|
|
ENST00000634433.2:c.4920T=
|
ENSP00000489431.2:p.Thr1640=
|
|
ENST00000644379.2:c.5109T=
|
ENSP00000496570.2:p.Thr1703=
|
|
ENST00000644555.2:c.1593T=
|
ENSP00000494614.2:p.Thr531=
|
|
ENST00000652672.2:c.4902T=
|
ENSP00000498906.2:p.Thr1634=
|
|
ENST00000484087.6:c.1605T=
|
ENSP00000419481.2:p.Thr535=
|
|
ENST00000357654.9:c.5043T=
MANE Select
|
ENSP00000350283.3:p.Thr1681=
|
|
ENST00000471181.7:c.5106T=
|
ENSP00000418960.2:p.Thr1702=
|
|
ENST00000644379.1:c.1430T=
|
|
|
ENST00000352993.7:c.1617T=
|
ENSP00000312236.5:p.Thr539=
|
|
ENST00000357654.7:c.5043T=
|
ENSP00000350283.3:p.Thr1681=
|
|
ENST00000461221.5:c.*4826T=
|
ENSP00000418548.1:n.*4826T=
|
|
ENST00000468300.5:c.1731T=
|
ENSP00000417148.1:p.Thr577=
|
|
ENST00000471181.6:c.5106T=
|
ENSP00000418960.2:p.Thr1702=
|
|
ENST00000472490.1:n.196T=
|
|
|
ENST00000478531.5:c.1731T=
|
ENSP00000420412.1:p.Thr577=
|
|
ENST00000484087.5:c.1356T=
|
ENSP00000419481.1:p.Thr452=
|
|
ENST00000491747.6:c.1731T=
|
ENSP00000420705.2:p.Thr577=
|
|
ENST00000493795.5:c.4902T=
|
ENSP00000418775.1:p.Thr1634=
|
|
ENST00000493919.5:c.1593T=
|
ENSP00000418819.1:p.Thr531=
|
|
ENST00000586385.5:c.5-3688T=
|
ENSP00000465818.1:n.5-3688T=
|
|
ENST00000591534.5:c.516T=
|
ENSP00000467329.1:p.Thr172=
|
|
ENST00000591849.5:c.-98-17449T=
|
ENSP00000465347.1:n.-98-17449T=
|
|
NM_007294.3:c.5043T= , LRG_292t1:c.5043T=
|
NP_009225.1:p.Thr1681=
|
|
NM_007297.3:c.4902T=
|
NP_009228.2:p.Thr1634=
|
|
NM_007298.3:c.1731T=
|
NP_009229.2:p.Thr577=
|
|
NM_007299.3:c.1731T=
|
NP_009230.2:p.Thr577=
|
|
NM_007300.3:c.5106T=
|
NP_009231.2:p.Thr1702=
|
|
NR_027676.1:n.5179T=
|
|
|
NM_007294.4:c.5043T=
MANE Select
|
NP_009225.1:p.Thr1681=
|
|
NM_007297.4:c.4902T=
|
NP_009228.2:p.Thr1634=
|
|
NM_007299.4:c.1731T=
|
NP_009230.2:p.Thr577=
|
|
NM_007300.4:c.5106T=
|
NP_009231.2:p.Thr1702=
|
|
NR_027676.2:n.5220T=
|
|
|