ENST00000461574.2:c.4126A=
|
ENSP00000417241.2:p.Thr1376=
|
|
ENST00000470026.6:c.4126A=
|
ENSP00000419274.2:p.Thr1376=
|
|
ENST00000473961.6:c.4000A=
|
ENSP00000420201.2:p.Thr1334=
|
|
ENST00000476777.6:c.4123A=
|
ENSP00000417554.2:p.Thr1375=
|
|
ENST00000477152.6:c.4048A=
|
ENSP00000419988.2:p.Thr1350=
|
|
ENST00000478531.6:c.814A=
|
ENSP00000420412.2:p.Thr272=
|
|
ENST00000489037.2:c.4048A=
|
ENSP00000420781.2:p.Thr1350=
|
|
ENST00000493919.6:c.676A=
|
ENSP00000418819.2:p.Thr226=
|
|
ENST00000494123.6:c.4126A=
|
ENSP00000419103.2:p.Thr1376=
|
|
ENST00000497488.2:c.3238A=
|
ENSP00000418986.2:p.Thr1080=
|
|
ENST00000618469.2:c.4126A=
|
ENSP00000478114.2:p.Thr1376=
|
|
ENST00000634433.2:c.4003A=
|
ENSP00000489431.2:p.Thr1335=
|
|
ENST00000644379.2:c.4126A=
|
ENSP00000496570.2:p.Thr1376=
|
|
ENST00000644555.2:c.676A=
|
ENSP00000494614.2:p.Thr226=
|
|
ENST00000652672.2:c.3985A=
|
ENSP00000498906.2:p.Thr1329=
|
|
ENST00000484087.6:c.694A=
|
ENSP00000419481.2:p.Thr232=
|
|
ENST00000700182.1:c.736A=
|
ENSP00000514849.1:p.Thr246=
|
|
ENST00000357654.9:c.4126A=
MANE Select
|
ENSP00000350283.3:p.Thr1376=
|
|
ENST00000471181.7:c.4126A=
|
ENSP00000418960.2:p.Thr1376=
|
|
ENST00000644379.1:c.447A=
|
|
|
ENST00000352993.7:c.700A=
|
ENSP00000312236.5:p.Thr234=
|
|
ENST00000357654.7:c.4126A=
|
ENSP00000350283.3:p.Thr1376=
|
|
ENST00000461221.5:c.*3909A=
|
ENSP00000418548.1:n.*3909A=
|
|
ENST00000461574.1:c.420A=
|
|
|
ENST00000468300.5:c.817A=
|
ENSP00000417148.1:p.Thr273=
|
|
ENST00000471181.6:c.4126A=
|
ENSP00000418960.2:p.Thr1376=
|
|
ENST00000478531.5:c.814A=
|
ENSP00000420412.1:p.Thr272=
|
|
ENST00000484087.5:c.439A=
|
ENSP00000419481.1:p.Thr147=
|
|
ENST00000487825.5:c.442A=
|
ENSP00000418212.1:p.Thr148=
|
|
ENST00000491747.6:c.817A=
|
ENSP00000420705.2:p.Thr273=
|
|
ENST00000493795.5:c.3985A=
|
ENSP00000418775.1:p.Thr1329=
|
|
ENST00000493919.5:c.676A=
|
ENSP00000418819.1:p.Thr226=
|
|
ENST00000586385.5:c.5-27052A=
|
ENSP00000465818.1:n.5-27052A=
|
|
ENST00000591534.5:c.-43-16482A=
|
ENSP00000467329.1:n.-43-16482A=
|
|
ENST00000591849.5:c.-99+34268A=
|
ENSP00000465347.1:n.-99+34268A=
|
|
NM_007294.3:c.4126A= , LRG_292t1:c.4126A=
|
NP_009225.1:p.Thr1376=
|
|
NM_007297.3:c.3985A=
|
NP_009228.2:p.Thr1329=
|
|
NM_007298.3:c.817A=
|
NP_009229.2:p.Thr273=
|
|
NM_007299.3:c.817A=
|
NP_009230.2:p.Thr273=
|
|
NM_007300.3:c.4126A=
|
NP_009231.2:p.Thr1376=
|
|
NR_027676.1:n.4262A=
|
|
|
NM_007294.4:c.4126A=
MANE Select
|
NP_009225.1:p.Thr1376=
|
|
NM_007297.4:c.3985A=
|
NP_009228.2:p.Thr1329=
|
|
NM_007299.4:c.817A=
|
NP_009230.2:p.Thr273=
|
|
NM_007300.4:c.4126A=
|
NP_009231.2:p.Thr1376=
|
|
NR_027676.2:n.4303A=
|
|
|