ENST00000703936.1:c.2783C>A
|
ENSP00000515567.1:p.Ala928Glu
|
|
ENST00000703937.1:c.*1844C>A
|
ENSP00000515568.1:n.*1844C>A
|
|
ENST00000326739.9:c.743C>A
MANE Select
|
ENSP00000321584.4:p.Ala248Glu
|
|
ENST00000429182.6:c.743C>A
|
ENSP00000393525.2:p.Ala248Glu
|
|
ENST00000442157.2:c.668C>A
|
ENSP00000403502.2:p.Ala223Glu
|
|
ENST00000462980.2:n.1258C>A
|
|
|
ENST00000472328.2:n.809C>A
|
|
|
ENST00000491610.2:n.703C>A
|
|
|
ENST00000676607.1:n.1039C>A
|
|
|
ENST00000676627.1:n.1473C>A
|
|
|
ENST00000676708.1:n.2023C>A
|
|
|
ENST00000676864.1:n.1892C>A
|
|
|
ENST00000677010.1:c.779C>A
|
ENSP00000503089.1:p.Ala260Glu
|
|
ENST00000677108.1:n.2649C>A
|
|
|
ENST00000677168.1:n.1215C>A
|
|
|
ENST00000677185.1:n.1306C>A
|
|
|
ENST00000677205.1:n.1527C>A
|
|
|
ENST00000677344.1:n.2017C>A
|
|
|
ENST00000677480.1:c.*420C>A
|
ENSP00000504378.1:n.*420C>A
|
|
ENST00000677519.1:n.1453C>A
|
|
|
ENST00000677593.1:n.1299C>A
|
|
|
ENST00000677740.1:n.2248C>A
|
|
|
ENST00000677991.1:n.1916C>A
|
|
|
ENST00000678001.1:n.1236C>A
|
|
|
ENST00000678085.1:n.1299C>A
|
|
|
ENST00000678177.1:n.2592C>A
|
|
|
ENST00000678603.1:n.1821C>A
|
|
|
ENST00000678724.1:c.668C>A
|
ENSP00000503874.1:p.Ala223Glu
|
|
ENST00000678920.1:n.901C>A
|
|
|
ENST00000679019.1:n.1513C>A
|
|
|
ENST00000679117.1:c.*558C>A
|
ENSP00000503240.1:n.*558C>A
|
|
ENST00000679339.1:n.1584C>A
|
|
|
ENST00000326739.8:c.743C>A
|
ENSP00000321584.4:p.Ala248Glu
|
|
ENST00000429182.5:c.537C>A
|
|
|
ENST00000442157.1:c.668C>A
|
ENSP00000403502.1:p.Ala223Glu
|
|
ENST00000462980.1:n.645C>A
|
|
|
ENST00000491610.1:n.703C>A
|
|
|
NM_000884.2:c.743C>A
|
NP_000875.2:p.Ala248Glu
|
|
XM_006713128.2:c.953C>A
|
XP_006713191.1:p.Ala318Glu
|
|
XM_006713128.3:c.953C>A
|
XP_006713191.1:p.Ala318Glu
|
|
XM_017006349.1:c.878C>A
|
XP_016861838.1:p.Ala293Glu
|
|
XM_017006350.1:c.878C>A
|
XP_016861839.1:p.Ala293Glu
|
|
NM_000884.3:c.743C>A
MANE Select
|
NP_000875.2:p.Ala248Glu
|
|