|
ENST00000359526.9:c.1824G>T
MANE Select
|
ENSP00000352516.3:p.Leu608=
|
|
|
ENST00000676604.1:n.1436G>T
|
|
|
|
ENST00000676610.1:c.1776G>T
|
ENSP00000504236.1:p.Leu592=
|
|
|
ENST00000676820.1:n.1832G>T
|
|
|
|
ENST00000676868.1:n.2460G>T
|
|
|
|
ENST00000677013.1:c.*1466G>T
|
ENSP00000503135.1:n.*1466G>T
|
|
|
ENST00000677250.1:c.*896G>T
|
ENSP00000502894.1:n.*896G>T
|
|
|
ENST00000677616.1:c.1467G>T
|
ENSP00000503055.1:p.Leu489=
|
|
|
ENST00000677634.1:c.1776G>T
|
ENSP00000504246.1:p.Leu592=
|
|
|
ENST00000677685.1:c.*1001G>T
|
ENSP00000503407.1:n.*1001G>T
|
|
|
ENST00000677783.1:n.2246G>T
|
|
|
|
ENST00000677946.1:c.1776G>T
|
ENSP00000504202.1:p.Leu592=
|
|
|
ENST00000678024.1:n.1919G>T
|
|
|
|
ENST00000678694.1:n.1097G>T
|
|
|
|
ENST00000678804.1:c.1776G>T
|
ENSP00000503853.1:p.Leu592=
|
|
|
ENST00000679103.1:c.1776G>T
|
ENSP00000503151.1:p.Leu592=
|
|
|
ENST00000679313.1:c.1776G>T
|
ENSP00000504512.1:p.Leu592=
|
|
|
ENST00000340748.8:c.1776G>T
|
ENSP00000345739.3:p.Leu592=
|
|
|
ENST00000359526.8:c.1824G>T
|
ENSP00000352516.3:p.Leu608=
|
|
|
ENST00000540357.5:c.768G>T
|
ENSP00000440457.2:p.Leu256=
|
|
|
ENST00000586799.1:c.210G>T
|
|
|
|
ENST00000592705.5:c.*1514G>T
|
ENSP00000466657.1:n.*1514G>T
|
|
|
NM_001130823.1:c.1824G>T , LRG_362t1:c.1824G>T
|
NP_001124295.1:p.Leu608=
|
|
|
NM_001379.2:c.1776G>T
|
NP_001370.1:p.Leu592=
|
|
|
XM_011527772.1:c.1824G>T
|
XP_011526074.1:p.Leu608=
|
|
|
XM_011527773.1:c.1776G>T
|
XP_011526075.1:p.Leu592=
|
|
|
XM_011527774.1:c.1413G>T
|
XP_011526076.1:p.Leu471=
|
|
|
NM_001130823.2:c.1824G>T
|
NP_001124295.1:p.Leu608=
|
|
|
NM_001318730.1:c.1776G>T
|
NP_001305659.1:p.Leu592=
|
|
|
NM_001318731.1:c.1461G>T
|
NP_001305660.1:p.Leu487=
|
|
|
NM_001379.3:c.1776G>T
|
NP_001370.1:p.Leu592=
|
|
|
NM_001130823.3:c.1824G>T
MANE Select
|
NP_001124295.1:p.Leu608=
|
|
|
NM_001318730.2:c.1776G>T
|
NP_001305659.1:p.Leu592=
|
|
|
NM_001318731.2:c.1461G>T
|
NP_001305660.1:p.Leu487=
|
|
|
NM_001379.4:c.1776G>T
|
NP_001370.1:p.Leu592=
|
|
