|
NM_001127208.3:c.3583A>G
(TET2)
MANE Select
|
NP_001120680.1:p.Ile1195Val
|
|
ENST00000380013.9:c.3583A>G
(TET2)
MANE Select
|
ENSP00000369351.4:p.Ile1195Val
|
|
NM_001127208.2:c.3583A>G , LRG_626t1:c.3583A>G
(TET2)
|
NP_001120680.1:p.Ile1195Val
|
|
NR_126420.1:n.319-65244T>C
(TET2-AS1)
|
|
|
ENST00000265149.9:c.3492A>G
(TET2)
|
ENSP00000265149.5:p.Leu1164=
|
|
ENST00000380013.8:c.3583A>G
(TET2)
|
ENSP00000369351.4:p.Ile1195Val
|
|
ENST00000513237.5:c.3646A>G
(TET2)
|
ENSP00000425443.1:p.Ile1216Val
|
|
ENST00000540549.5:c.3583A>G
(TET2)
|
ENSP00000442788.1:p.Ile1195Val
|
|
XM_005263082.1:c.3583A>G
(TET2)
|
XP_005263139.1:p.Ile1195Val
|
|
XM_005263082.3:c.3583A>G
(TET2)
|
XP_005263139.1:p.Ile1195Val
|
|
XM_006714242.2:c.3492A>G
(TET2)
|
XP_006714305.1:p.Leu1164=
|
|
XM_006714242.3:c.3492A>G
(TET2)
|
XP_006714305.1:p.Leu1164=
|
|
XM_011532044.1:c.94A>G
(TET2)
|
XP_011530346.1:p.Ile32Val
|
|
XM_024454102.1:c.3583A>G
(TET2)
|
XP_024309870.1:p.Ile1195Val
|
|
XM_024454103.1:c.3583A>G
(TET2)
|
XP_024309871.1:p.Ile1195Val
|
|
XR_001741246.1:n.3953A>G
(TET2)
|
|
|
XR_244633.2:n.3705+5565A>G
(TET2)
|
|
|
XR_244633.3:n.3740+5565A>G
(TET2)
|
|
|
XR_244634.2:n.3788A>G
(TET2)
|
|
|
XR_427546.2:n.3879A>G
(TET2)
|
|
|
XR_427546.4:n.3914A>G
(TET2)
|
|
|
XR_938746.1:n.4079A>G
(TET2)
|
|
|
XR_938746.2:n.4114A>G
(TET2)
|
|
|
XR_938747.1:n.4009A>G
(TET2)
|
|
|
XR_938747.3:n.4044A>G
(TET2)
|
|