ENST00000478630.2:n.3192G>A
|
|
|
ENST00000674112.2:c.*314G>A
|
ENSP00000501166.2:n.*314G>A
|
|
ENST00000683242.1:n.1519G>A
|
|
|
ENST00000685042.1:c.*1628G>A
|
ENSP00000509871.1:n.*1628G>A
|
|
ENST00000686442.1:n.5850G>A
|
|
|
ENST00000689256.1:n.5549G>A
|
|
|
ENST00000690231.1:c.4972G>A
|
ENSP00000508461.1:p.Glu1658Lys
|
|
ENST00000692002.1:c.997G>A
|
ENSP00000508567.1:p.Glu333Lys
|
|
ENST00000265348.9:c.4972G>A
MANE Select
|
ENSP00000265348.4:p.Glu1658Lys
|
|
ENST00000674100.1:c.5068G>A
|
ENSP00000501292.1:p.Glu1690Lys
|
|
ENST00000674112.1:c.3453G>A
|
|
|
ENST00000674134.1:c.5068G>A
|
ENSP00000501068.1:p.Glu1690Lys
|
|
ENST00000265348.7:c.4972G>A
|
ENSP00000265348.3:p.Glu1658Lys
|
|
ENST00000535468.1:c.5224G>A
|
ENSP00000438788.1:p.Glu1742Lys
|
|
NM_001168370.1:c.5224G>A
|
NP_001161842.1:p.Glu1742Lys
|
|
NM_014780.4:c.4972G>A
|
NP_055595.2:p.Glu1658Lys
|
|
XM_005249503.1:c.5128G>A
|
XP_005249560.1:p.Glu1710Lys
|
|
XM_006715285.1:c.5080G>A
|
XP_006715348.1:p.Glu1694Lys
|
|
XM_011515019.1:c.5236G>A
|
XP_011513321.1:p.Glu1746Lys
|
|
XM_011515020.1:c.5140G>A
|
XP_011513322.1:p.Glu1714Lys
|
|
XM_011515021.1:c.2845G>A
|
XP_011513323.1:p.Glu949Lys
|
|
XM_005249503.3:c.5128G>A
|
XP_005249560.1:p.Glu1710Lys
|
|
XM_006715285.2:c.5080G>A
|
XP_006715348.1:p.Glu1694Lys
|
|
XM_011515019.2:c.5236G>A
|
XP_011513321.1:p.Glu1746Lys
|
|
XM_011515020.2:c.5140G>A
|
XP_011513322.1:p.Glu1714Lys
|
|
XM_017011533.1:c.5263G>A
|
XP_016867022.1:p.Glu1755Lys
|
|
XM_017011534.1:c.5251G>A
|
XP_016867023.1:p.Glu1751Lys
|
|
XM_017011535.1:c.5167G>A
|
XP_016867024.1:p.Glu1723Lys
|
|
XM_017011536.2:c.5107G>A
|
XP_016867025.1:p.Glu1703Lys
|
|
XM_017011537.2:c.5068G>A
|
XP_016867026.1:p.Glu1690Lys
|
|
XM_017011538.2:c.5011G>A
|
XP_016867027.1:p.Glu1671Lys
|
|
XM_017011539.2:c.4984G>A
|
XP_016867028.1:p.Glu1662Lys
|
|
NM_001168370.2:c.5068G>A
|
NP_001161842.2:p.Glu1690Lys
|
|
NM_001374872.1:c.5068G>A
|
NP_001361801.1:p.Glu1690Lys
|
|
NM_001374873.1:c.4984G>A
|
NP_001361802.1:p.Glu1662Lys
|
|
NM_001374874.1:c.4969G>A
|
NP_001361803.1:p.Glu1657Lys
|
|
NM_014780.5:c.4972G>A
MANE Select
|
NP_055595.2:p.Glu1658Lys
|
|