ENST00000224721.12:c.8317G>T
MANE Select
|
ENSP00000224721.9:p.Glu2773Ter
|
|
ENST00000642965.1:c.2250G>T
|
ENSP00000495222.1:n.2250G>T
|
|
ENST00000647092.1:c.1914G>T
|
ENSP00000495176.1:n.1914G>T
|
|
ENST00000224721.10:c.8332G>T
|
ENSP00000224721.8:p.Glu2778Ter
|
|
ENST00000398788.4:c.1597G>T
|
ENSP00000381768.3:p.Glu533Ter
|
|
ENST00000475158.1:n.1853G>T
|
|
|
ENST00000619887.4:c.1597G>T
|
ENSP00000478374.1:p.Glu533Ter
|
|
ENST00000622827.4:c.8317G>T
|
ENSP00000483211.1:p.Glu2773Ter
|
|
NM_001171933.1:c.1597G>T
|
NP_001165404.1:p.Glu533Ter
|
|
NM_001171934.1:c.1597G>T
|
NP_001165405.1:p.Glu533Ter
|
|
NM_022124.5:c.8317G>T
|
NP_071407.4:p.Glu2773Ter
|
|
XM_006717940.2:c.8512G>T
|
XP_006718003.1:p.Glu2838Ter
|
|
XM_006717942.2:c.8446G>T
|
XP_006718005.1:p.Glu2816Ter
|
|
XM_011540039.1:c.8509G>T
|
XP_011538341.1:p.Glu2837Ter
|
|
XM_011540040.1:c.8506G>T
|
XP_011538342.1:p.Glu2836Ter
|
|
XM_011540041.1:c.8452G>T
|
XP_011538343.1:p.Glu2818Ter
|
|
XM_011540042.1:c.8422G>T
|
XP_011538344.1:p.Glu2808Ter
|
|
XM_011540043.1:c.8512G>T
|
XP_011538345.1:p.Glu2838Ter
|
|
XM_011540044.1:c.8377G>T
|
XP_011538346.1:p.Glu2793Ter
|
|
XM_011540045.1:c.8512G>T
|
XP_011538347.1:p.Glu2838Ter
|
|
XM_011540046.1:c.7972G>T
|
XP_011538348.1:p.Glu2658Ter
|
|
XM_011540047.1:c.7330G>T
|
XP_011538349.1:p.Glu2444Ter
|
|
XM_011540052.1:c.4840G>T
|
XP_011538354.1:p.Glu1614Ter
|
|
NM_022124.6:c.8317G>T
MANE Select
|
NP_071407.4:p.Glu2773Ter
|
|