ENST00000359637.3:c.1047C>T
|
ENSP00000352658.2:p.Asp349=
|
|
ENST00000470918.2:n.1505C>T
|
|
|
ENST00000695968.1:c.1056C>T
|
ENSP00000512295.1:p.Asp352=
|
|
ENST00000695969.1:c.1239C>T
|
ENSP00000512296.1:p.Asp413=
|
|
ENST00000695970.1:c.1239C>T
|
ENSP00000512297.1:p.Asp413=
|
|
ENST00000695971.1:c.1218C>T
|
ENSP00000512298.1:p.Asp406=
|
|
ENST00000695972.1:c.1239C>T
|
ENSP00000512299.1:p.Asp413=
|
|
ENST00000695973.1:c.1239C>T
|
ENSP00000512300.1:p.Asp413=
|
|
ENST00000695974.1:c.1239C>T
|
ENSP00000512301.1:p.Asp413=
|
|
ENST00000695975.1:c.1239C>T
|
ENSP00000512302.1:p.Asp413=
|
|
ENST00000695976.1:c.1050C>T
|
ENSP00000512303.1:p.Asp350=
|
|
ENST00000695977.1:n.80C>T
|
|
|
ENST00000695978.1:c.1239C>T
|
ENSP00000512304.1:p.Asp413=
|
|
ENST00000695979.1:c.1218C>T
|
ENSP00000512305.1:p.Asp406=
|
|
ENST00000695980.1:n.1359C>T
|
|
|
ENST00000695981.1:c.1239C>T
|
ENSP00000512306.1:p.Asp413=
|
|
ENST00000695983.1:c.1239C>T
|
ENSP00000512308.1:p.Asp413=
|
|
ENST00000695984.1:c.244+16979C>T
|
ENSP00000512309.1:n.244+16979C>T
|
|
ENST00000695986.1:c.*890C>T
|
ENSP00000512311.1:n.*890C>T
|
|
ENST00000695987.1:c.1050C>T
|
ENSP00000512312.1:p.Asp350=
|
|
ENST00000696018.1:n.1323C>T
|
|
|
ENST00000696019.1:n.1323C>T
|
|
|
ENST00000696020.1:n.1323C>T
|
|
|
ENST00000696021.1:n.1302C>T
|
|
|
ENST00000696022.1:n.1323C>T
|
|
|
ENST00000696023.1:c.1239C>T
|
ENSP00000512334.1:p.Asp413=
|
|
ENST00000696024.1:n.1323C>T
|
|
|
ENST00000696025.1:n.1323C>T
|
|
|
ENST00000696026.1:c.1239C>T
|
ENSP00000512335.1:p.Asp413=
|
|
ENST00000696027.1:c.1239C>T
|
ENSP00000512336.1:p.Asp413=
|
|
ENST00000696028.1:c.1239C>T
|
ENSP00000512337.1:p.Asp413=
|
|
ENST00000696029.1:c.1239C>T
|
ENSP00000512338.1:p.Asp413=
|
|
ENST00000696030.1:c.1164C>T
|
ENSP00000512339.1:p.Asp388=
|
|
ENST00000696031.1:c.*757C>T
|
ENSP00000512340.1:n.*757C>T
|
|
ENST00000696032.1:c.1239C>T
|
ENSP00000512341.1:p.Asp413=
|
|
ENST00000696033.1:c.1159+528C>T
|
ENSP00000512342.1:n.1159+528C>T
|
|
ENST00000367429.9:c.1239C>T
MANE Select
|
ENSP00000356399.4:p.Asp413=
|
|
ENST00000359637.2:c.1047C>T
|
ENSP00000352658.2:p.Asp349=
|
|
ENST00000367429.8:c.1239C>T
|
ENSP00000356399.4:p.Asp413=
|
|
ENST00000466229.5:n.3255C>T
|
|
|
ENST00000630130.2:c.1239C>T
|
ENSP00000487250.1:p.Asp413=
|
|
NM_000186.3:c.1239C>T , LRG_47t1:c.1239C>T
|
NP_000177.2:p.Asp413=
|
|
NM_001014975.2:c.1239C>T
|
NP_001014975.1:p.Asp413=
|
|
XM_017001108.2:c.1239C>T
|
XP_016856597.1:p.Asp413=
|
|
XR_001737134.2:n.1324C>T
|
|
|
NM_000186.4:c.1239C>T
MANE Select
|
NP_000177.2:p.Asp413=
|
|
NM_001014975.3:c.1239C>T
|
NP_001014975.1:p.Asp413=
|
|