ENST00000224721.12:c.7564G>T
MANE Select
|
ENSP00000224721.9:p.Glu2522Ter
|
|
ENST00000642965.1:c.1497G>T
|
ENSP00000495222.1:n.1497G>T
|
|
ENST00000647092.1:c.1161G>T
|
ENSP00000495176.1:n.1161G>T
|
|
ENST00000224721.10:c.7579G>T
|
ENSP00000224721.8:p.Glu2527Ter
|
|
ENST00000398788.4:c.844G>T
|
ENSP00000381768.3:p.Glu282Ter
|
|
ENST00000475158.1:n.1100G>T
|
|
|
ENST00000619887.4:c.844G>T
|
ENSP00000478374.1:p.Glu282Ter
|
|
ENST00000622827.4:c.7564G>T
|
ENSP00000483211.1:p.Glu2522Ter
|
|
NM_001171933.1:c.844G>T
|
NP_001165404.1:p.Glu282Ter
|
|
NM_001171934.1:c.844G>T
|
NP_001165405.1:p.Glu282Ter
|
|
NM_022124.5:c.7564G>T
|
NP_071407.4:p.Glu2522Ter
|
|
XM_006717940.2:c.7759G>T
|
XP_006718003.1:p.Glu2587Ter
|
|
XM_006717942.2:c.7693G>T
|
XP_006718005.1:p.Glu2565Ter
|
|
XM_011540039.1:c.7756G>T
|
XP_011538341.1:p.Glu2586Ter
|
|
XM_011540040.1:c.7753G>T
|
XP_011538342.1:p.Glu2585Ter
|
|
XM_011540041.1:c.7699G>T
|
XP_011538343.1:p.Glu2567Ter
|
|
XM_011540042.1:c.7669G>T
|
XP_011538344.1:p.Glu2557Ter
|
|
XM_011540043.1:c.7759G>T
|
XP_011538345.1:p.Glu2587Ter
|
|
XM_011540044.1:c.7624G>T
|
XP_011538346.1:p.Glu2542Ter
|
|
XM_011540045.1:c.7759G>T
|
XP_011538347.1:p.Glu2587Ter
|
|
XM_011540046.1:c.7219G>T
|
XP_011538348.1:p.Glu2407Ter
|
|
XM_011540047.1:c.6577G>T
|
XP_011538349.1:p.Glu2193Ter
|
|
XM_011540052.1:c.4087G>T
|
XP_011538354.1:p.Glu1363Ter
|
|
NM_022124.6:c.7564G>T
MANE Select
|
NP_071407.4:p.Glu2522Ter
|
|