ENST00000470918.2:n.4553A>T
|
|
|
ENST00000695970.1:c.3351A>T
|
ENSP00000512297.1:p.Glu1117Asp
|
|
ENST00000695971.1:c.3504A>T
|
ENSP00000512298.1:p.Glu1168Asp
|
|
ENST00000695972.1:c.*602A>T
|
ENSP00000512299.1:n.*602A>T
|
|
ENST00000695973.1:c.*1889A>T
|
ENSP00000512300.1:n.*1889A>T
|
|
ENST00000695974.1:c.3348A>T
|
ENSP00000512301.1:p.Glu1116Asp
|
|
ENST00000695975.1:c.*1652A>T
|
ENSP00000512302.1:n.*1652A>T
|
|
ENST00000695976.1:c.3336A>T
|
ENSP00000512303.1:p.Glu1112Asp
|
|
ENST00000695981.1:c.3525A>T
|
ENSP00000512306.1:p.Glu1175Asp
|
|
ENST00000695984.1:c.1533A>T
|
ENSP00000512309.1:p.Glu511Asp
|
|
ENST00000695986.1:c.*3176A>T
|
ENSP00000512311.1:n.*3176A>T
|
|
ENST00000695990.1:n.559A>T
|
|
|
ENST00000696026.1:c.*1807A>T
|
ENSP00000512335.1:n.*1807A>T
|
|
ENST00000696027.1:c.3519A>T
|
ENSP00000512336.1:p.Glu1173Asp
|
|
ENST00000696028.1:c.3453A>T
|
ENSP00000512337.1:p.Glu1151Asp
|
|
ENST00000696029.1:c.3519A>T
|
ENSP00000512338.1:p.Glu1173Asp
|
|
ENST00000696031.1:c.*3043A>T
|
ENSP00000512340.1:n.*3043A>T
|
|
ENST00000696032.1:c.3525A>T
|
ENSP00000512341.1:p.Glu1175Asp
|
|
ENST00000696033.1:c.1160-32655A>T
|
ENSP00000512342.1:n.1160-32655A>T
|
|
ENST00000367429.9:c.3525A>T
MANE Select
|
ENSP00000356399.4:p.Glu1175Asp
|
|
ENST00000367429.8:c.3525A>T
|
ENSP00000356399.4:p.Glu1175Asp
|
|
ENST00000466229.5:n.6623A>T
|
|
|
NM_000186.3:c.3525A>T , LRG_47t1:c.3525A>T
|
NP_000177.2:p.Glu1175Asp
|
|
XR_001737134.2:n.3711A>T
|
|
|
NM_000186.4:c.3525A>T
MANE Select
|
NP_000177.2:p.Glu1175Asp
|
|