ENST00000261304.7:c.1507G=
MANE Select
|
ENSP00000261304.2:p.Glu503=
|
|
ENST00000261304.6:c.1507G=
|
ENSP00000261304.2:p.Glu503=
|
|
ENST00000393568.8:c.1438G=
|
ENSP00000377198.4:p.Glu480=
|
|
ENST00000393569.6:c.1429G=
|
ENSP00000377199.2:p.Glu477=
|
|
ENST00000544807.6:c.1339G=
|
ENSP00000437513.2:p.Glu447=
|
|
ENST00000555000.5:c.874G=
|
ENSP00000450472.1:p.Glu292=
|
|
ENST00000555179.1:c.206+2012G=
|
|
|
ENST00000557316.5:c.*905G=
|
ENSP00000452314.1:n.*905G=
|
|
NM_000153.3:c.1507G=
|
NP_000144.2:p.Glu503=
|
|
NM_001201401.1:c.1438G=
|
NP_001188330.1:p.Glu480=
|
|
NM_001201402.1:c.1429G=
|
NP_001188331.1:p.Glu477=
|
|
XM_011536618.1:c.1339G=
|
XP_011534920.1:p.Glu447=
|
|
XM_011536618.2:c.1339G=
|
XP_011534920.1:p.Glu447=
|
|
NM_000153.4:c.1507G=
MANE Select
|
NP_000144.2:p.Glu503=
|
|
NM_001201401.2:c.1438G=
|
NP_001188330.1:p.Glu480=
|
|
NM_001201402.2:c.1429G=
|
NP_001188331.1:p.Glu477=
|
|