ENST00000389266.8:c.804T>G
MANE Select
|
ENSP00000373918.3:p.Thr268=
|
|
ENST00000444666.6:c.804T>G
|
ENSP00000415447.2:p.Thr268=
|
|
ENST00000470392.2:n.894T>G
|
|
|
ENST00000478124.6:n.867T>G
|
|
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ENST00000485784.2:n.883T>G
|
|
|
ENST00000674616.1:c.*518T>G
|
ENSP00000502408.1:n.*518T>G
|
|
ENST00000674643.1:c.804T>G
|
ENSP00000501636.1:p.Thr268=
|
|
ENST00000674734.1:n.1300T>G
|
|
|
ENST00000674737.1:c.*142T>G
|
ENSP00000502464.1:n.*142T>G
|
|
ENST00000674807.1:c.804T>G
|
ENSP00000502814.1:p.Thr268=
|
|
ENST00000674815.1:c.435T>G
|
ENSP00000502799.1:p.Thr145=
|
|
ENST00000674851.1:c.435T>G
|
ENSP00000502451.1:p.Thr145=
|
|
ENST00000674969.1:n.2677T>G
|
|
|
ENST00000675051.1:c.603T>G
|
ENSP00000502296.1:p.Thr201=
|
|
ENST00000675529.1:c.*674T>G
|
ENSP00000501655.1:n.*674T>G
|
|
ENST00000675587.1:n.820T>G
|
|
|
ENST00000675651.1:c.804T>G
|
ENSP00000502513.1:p.Thr268=
|
|
ENST00000675693.1:c.636T>G
|
ENSP00000502174.1:p.Thr212=
|
|
ENST00000675810.1:c.702T>G
|
ENSP00000502743.1:p.Thr234=
|
|
ENST00000675859.1:c.804T>G
|
ENSP00000502033.1:p.Thr268=
|
|
ENST00000675863.1:n.812T>G
|
|
|
ENST00000675886.1:n.6844T>G
|
|
|
ENST00000676088.1:c.*746T>G
|
ENSP00000501884.1:n.*746T>G
|
|
ENST00000676140.1:c.804T>G
|
ENSP00000502571.1:p.Thr268=
|
|
ENST00000676164.1:c.*255T>G
|
ENSP00000501986.1:n.*255T>G
|
|
ENST00000676210.1:c.*93T>G
|
ENSP00000502373.1:n.*93T>G
|
|
ENST00000676259.1:c.*236T>G
|
ENSP00000501980.1:n.*236T>G
|
|
ENST00000676403.1:c.804T>G
|
ENSP00000502681.1:p.Thr268=
|
|
ENST00000389266.7:c.804T>G
|
ENSP00000373918.3:p.Thr268=
|
|
ENST00000478124.5:n.842T>G
|
|
|
NM_001316772.1:c.642T>G
|
NP_001303701.1:p.Thr214=
|
|
NM_002047.2:c.804T>G , LRG_243t1:c.804T>G
|
NP_002038.2:p.Thr268=
|
|
NM_002047.3:c.804T>G
|
NP_002038.2:p.Thr268=
|
|
XM_006715686.1:c.435T>G
|
XP_006715749.1:p.Thr145=
|
|
XM_006715686.2:c.435T>G
|
XP_006715749.1:p.Thr145=
|
|
NM_002047.4:c.804T>G
MANE Select
|
NP_002038.2:p.Thr268=
|
|