ENST00000389266.8:c.1031+98G>T
MANE Select
|
ENSP00000373918.3:n.1031+98G>T
|
|
ENST00000444666.6:c.1031+98G>T
|
ENSP00000415447.2:n.1031+98G>T
|
|
ENST00000470392.2:n.1121+98G>T
|
|
|
ENST00000478124.6:n.1094+98G>T
|
|
|
ENST00000485784.2:n.1110+98G>T
|
|
|
ENST00000674616.1:c.*745+98G>T
|
ENSP00000502408.1:n.*745+98G>T
|
|
ENST00000674643.1:c.1031+98G>T
|
ENSP00000501636.1:n.1031+98G>T
|
|
ENST00000674734.1:n.1527+98G>T
|
|
|
ENST00000674737.1:c.*369+98G>T
|
ENSP00000502464.1:n.*369+98G>T
|
|
ENST00000674807.1:c.1031+98G>T
|
ENSP00000502814.1:n.1031+98G>T
|
|
ENST00000674815.1:c.662+98G>T
|
ENSP00000502799.1:n.662+98G>T
|
|
ENST00000674851.1:c.662+98G>T
|
ENSP00000502451.1:n.662+98G>T
|
|
ENST00000674969.1:n.2904+98G>T
|
|
|
ENST00000675051.1:c.830+98G>T
|
ENSP00000502296.1:n.830+98G>T
|
|
ENST00000675529.1:c.*901+98G>T
|
ENSP00000501655.1:n.*901+98G>T
|
|
ENST00000675587.1:n.1047+98G>T
|
|
|
ENST00000675651.1:c.1031+98G>T
|
ENSP00000502513.1:n.1031+98G>T
|
|
ENST00000675693.1:c.863+98G>T
|
ENSP00000502174.1:n.863+98G>T
|
|
ENST00000675810.1:c.929+98G>T
|
ENSP00000502743.1:n.929+98G>T
|
|
ENST00000675859.1:c.1031+98G>T
|
ENSP00000502033.1:n.1031+98G>T
|
|
ENST00000675863.1:n.1039+98G>T
|
|
|
ENST00000675886.1:n.7071+98G>T
|
|
|
ENST00000676088.1:c.*973+98G>T
|
ENSP00000501884.1:n.*973+98G>T
|
|
ENST00000676140.1:c.1031+98G>T
|
ENSP00000502571.1:n.1031+98G>T
|
|
ENST00000676164.1:c.*482+98G>T
|
ENSP00000501986.1:n.*482+98G>T
|
|
ENST00000676210.1:c.*320+98G>T
|
ENSP00000502373.1:n.*320+98G>T
|
|
ENST00000676259.1:c.*463+98G>T
|
ENSP00000501980.1:n.*463+98G>T
|
|
ENST00000676403.1:c.1031+98G>T
|
ENSP00000502681.1:n.1031+98G>T
|
|
ENST00000389266.7:c.1031+98G>T
|
ENSP00000373918.3:n.1031+98G>T
|
|
ENST00000478124.5:n.1069+98G>T
|
|
|
NM_001316772.1:c.869+98G>T
|
NP_001303701.1:n.869+98G>T
|
|
NM_002047.2:c.1031+98G>T , LRG_243t1:c.1031+98G>T
|
NP_002038.2:n.1031+98G>T
|
|
NM_002047.3:c.1031+98G>T
|
NP_002038.2:n.1031+98G>T
|
|
XM_006715686.1:c.662+98G>T
|
XP_006715749.1:n.662+98G>T
|
|
XM_006715686.2:c.662+98G>T
|
XP_006715749.1:n.662+98G>T
|
|
NM_002047.4:c.1031+98G>T
MANE Select
|
NP_002038.2:n.1031+98G>T
|
|