ENST00000430710.8:c.2175G>A
|
ENSP00000406288.3:p.Glu725=
|
|
ENST00000555935.2:c.688G>A
|
|
|
ENST00000555962.6:c.-110-2718G>A
|
ENSP00000495174.1:n.-110-2718G>A
|
|
ENST00000557364.6:c.3012G>A
|
ENSP00000451601.1:p.Glu1004=
|
|
ENST00000643469.1:c.3012G>A
|
ENSP00000495070.1:p.Glu1004=
|
|
ENST00000645140.1:c.2924G>A
|
|
|
ENST00000645206.1:n.1526G>A
|
|
|
ENST00000645929.1:c.2175G>A
|
ENSP00000494402.1:p.Glu725=
|
|
ENST00000646340.1:c.3018G>A
|
ENSP00000496730.1:p.Glu1006=
|
|
ENST00000646647.2:c.3012G>A
MANE Select
|
ENSP00000495240.1:p.Glu1004=
|
|
ENST00000399982.6:c.3012G>A
|
ENSP00000382863.2:p.Glu1004=
|
|
ENST00000430710.7:c.2175G>A
|
ENSP00000406288.3:p.Glu725=
|
|
ENST00000555935.1:c.688G>A
|
|
|
ENST00000555962.5:n.151-2718G>A
|
|
|
ENST00000557364.5:c.3012G>A
|
ENSP00000451601.1:p.Glu1004=
|
|
NM_001170629.1:c.3012G>A
|
NP_001164100.1:p.Glu1004=
|
|
NM_020920.3:c.2175G>A
|
NP_065971.2:p.Glu725=
|
|
NM_001170629.2:c.3012G>A
MANE Select
|
NP_001164100.1:p.Glu1004=
|
|
NM_020920.4:c.2175G>A
|
NP_065971.2:p.Glu725=
|
|