ENST00000224721.12:c.7239G>A
MANE Select
|
ENSP00000224721.9:p.Glu2413=
|
|
ENST00000642965.1:c.1172G>A
|
ENSP00000495222.1:n.1172G>A
|
|
ENST00000647092.1:c.836G>A
|
ENSP00000495176.1:n.836G>A
|
|
ENST00000224721.10:c.7254G>A
|
ENSP00000224721.8:p.Glu2418=
|
|
ENST00000398788.4:c.519G>A
|
ENSP00000381768.3:p.Glu173=
|
|
ENST00000475158.1:n.775G>A
|
|
|
ENST00000619887.4:c.519G>A
|
ENSP00000478374.1:p.Glu173=
|
|
ENST00000622827.4:c.7239G>A
|
ENSP00000483211.1:p.Glu2413=
|
|
NM_001171933.1:c.519G>A
|
NP_001165404.1:p.Glu173=
|
|
NM_001171934.1:c.519G>A
|
NP_001165405.1:p.Glu173=
|
|
NM_022124.5:c.7239G>A
|
NP_071407.4:p.Glu2413=
|
|
XM_006717940.2:c.7434G>A
|
XP_006718003.1:p.Glu2478=
|
|
XM_006717942.2:c.7368G>A
|
XP_006718005.1:p.Glu2456=
|
|
XM_011540039.1:c.7431G>A
|
XP_011538341.1:p.Glu2477=
|
|
XM_011540040.1:c.7428G>A
|
XP_011538342.1:p.Glu2476=
|
|
XM_011540041.1:c.7374G>A
|
XP_011538343.1:p.Glu2458=
|
|
XM_011540042.1:c.7344G>A
|
XP_011538344.1:p.Glu2448=
|
|
XM_011540043.1:c.7434G>A
|
XP_011538345.1:p.Glu2478=
|
|
XM_011540044.1:c.7299G>A
|
XP_011538346.1:p.Glu2433=
|
|
XM_011540045.1:c.7434G>A
|
XP_011538347.1:p.Glu2478=
|
|
XM_011540046.1:c.6894G>A
|
XP_011538348.1:p.Glu2298=
|
|
XM_011540047.1:c.6252G>A
|
XP_011538349.1:p.Glu2084=
|
|
XM_011540052.1:c.3762G>A
|
XP_011538354.1:p.Glu1254=
|
|
NM_022124.6:c.7239G>A
MANE Select
|
NP_071407.4:p.Glu2413=
|
|