ENST00000389266.8:c.851C>T
MANE Select
|
ENSP00000373918.3:p.Thr284Ile
|
|
ENST00000444666.6:c.851C>T
|
ENSP00000415447.2:p.Thr284Ile
|
|
ENST00000470392.2:n.941C>T
|
|
|
ENST00000478124.6:n.914C>T
|
|
|
ENST00000485784.2:n.930C>T
|
|
|
ENST00000674616.1:c.*565C>T
|
ENSP00000502408.1:n.*565C>T
|
|
ENST00000674643.1:c.851C>T
|
ENSP00000501636.1:p.Thr284Ile
|
|
ENST00000674734.1:n.1347C>T
|
|
|
ENST00000674737.1:c.*189C>T
|
ENSP00000502464.1:n.*189C>T
|
|
ENST00000674807.1:c.851C>T
|
ENSP00000502814.1:p.Thr284Ile
|
|
ENST00000674815.1:c.482C>T
|
ENSP00000502799.1:p.Thr161Ile
|
|
ENST00000674851.1:c.482C>T
|
ENSP00000502451.1:p.Thr161Ile
|
|
ENST00000674969.1:n.2724C>T
|
|
|
ENST00000675051.1:c.650C>T
|
ENSP00000502296.1:p.Thr217Ile
|
|
ENST00000675529.1:c.*721C>T
|
ENSP00000501655.1:n.*721C>T
|
|
ENST00000675587.1:n.867C>T
|
|
|
ENST00000675651.1:c.851C>T
|
ENSP00000502513.1:p.Thr284Ile
|
|
ENST00000675693.1:c.683C>T
|
ENSP00000502174.1:p.Thr228Ile
|
|
ENST00000675810.1:c.749C>T
|
ENSP00000502743.1:p.Thr250Ile
|
|
ENST00000675859.1:c.851C>T
|
ENSP00000502033.1:p.Thr284Ile
|
|
ENST00000675863.1:n.859C>T
|
|
|
ENST00000675886.1:n.6891C>T
|
|
|
ENST00000676088.1:c.*793C>T
|
ENSP00000501884.1:n.*793C>T
|
|
ENST00000676140.1:c.851C>T
|
ENSP00000502571.1:p.Thr284Ile
|
|
ENST00000676164.1:c.*302C>T
|
ENSP00000501986.1:n.*302C>T
|
|
ENST00000676210.1:c.*140C>T
|
ENSP00000502373.1:n.*140C>T
|
|
ENST00000676259.1:c.*283C>T
|
ENSP00000501980.1:n.*283C>T
|
|
ENST00000676403.1:c.851C>T
|
ENSP00000502681.1:p.Thr284Ile
|
|
ENST00000389266.7:c.851C>T
|
ENSP00000373918.3:p.Thr284Ile
|
|
ENST00000478124.5:n.889C>T
|
|
|
NM_001316772.1:c.689C>T
|
NP_001303701.1:p.Thr230Ile
|
|
NM_002047.2:c.851C>T , LRG_243t1:c.851C>T
|
NP_002038.2:p.Thr284Ile
|
|
NM_002047.3:c.851C>T
|
NP_002038.2:p.Thr284Ile
|
|
XM_006715686.1:c.482C>T
|
XP_006715749.1:p.Thr161Ile
|
|
XM_006715686.2:c.482C>T
|
XP_006715749.1:p.Thr161Ile
|
|
NM_002047.4:c.851C>T
MANE Select
|
NP_002038.2:p.Thr284Ile
|
|