|
NM_001127208.3:c.4354C>T
(TET2)
MANE Select
|
NP_001120680.1:p.Arg1452Ter
|
|
ENST00000380013.9:c.4354C>T
(TET2)
MANE Select
|
ENSP00000369351.4:p.Arg1452Ter
|
|
NM_001127208.2:c.4354C>T , LRG_626t1:c.4354C>T
(TET2)
|
NP_001120680.1:p.Arg1452Ter
|
|
NR_126420.1:n.318+61651G>A
(TET2-AS1)
|
|
|
ENST00000265149.9:c.*678C>T
(TET2)
|
ENSP00000265149.5:n.*678C>T
|
|
ENST00000380013.8:c.4354C>T
(TET2)
|
ENSP00000369351.4:p.Arg1452Ter
|
|
ENST00000513237.5:c.4417C>T
(TET2)
|
ENSP00000425443.1:p.Arg1473Ter
|
|
ENST00000540549.5:c.4354C>T
(TET2)
|
ENSP00000442788.1:p.Arg1452Ter
|
|
XM_005263082.1:c.4354C>T
(TET2)
|
XP_005263139.1:p.Arg1452Ter
|
|
XM_005263082.3:c.4354C>T
(TET2)
|
XP_005263139.1:p.Arg1452Ter
|
|
XM_006714242.2:c.4054C>T
(TET2)
|
XP_006714305.1:p.Arg1352Ter
|
|
XM_006714242.3:c.4054C>T
(TET2)
|
XP_006714305.1:p.Arg1352Ter
|
|
XM_011532044.1:c.865C>T
(TET2)
|
XP_011530346.1:p.Arg289Ter
|
|
XM_024454102.1:c.4354C>T
(TET2)
|
XP_024309870.1:p.Arg1452Ter
|
|
XM_024454103.1:c.4354C>T
(TET2)
|
XP_024309871.1:p.Arg1452Ter
|
|
XR_244633.2:n.4256C>T
(TET2)
|
|
|
XR_244633.3:n.4291C>T
(TET2)
|
|
|
XR_244634.2:n.4559C>T
(TET2)
|
|
|
XR_427546.2:n.4441C>T
(TET2)
|
|
|
XR_427546.4:n.4476C>T
(TET2)
|
|
