ENST00000554192.6:c.1224G>T
|
ENSP00000450681.3:p.Glu408Asp
|
|
ENST00000554585.6:c.*149G>T
|
ENSP00000481526.2:n.*149G>T
|
|
ENST00000555458.6:c.1323G>T
|
ENSP00000451470.3:p.Glu441Asp
|
|
ENST00000553797.2:c.1398G>T
|
ENSP00000507566.1:p.Glu466Asp
|
|
ENST00000554826.2:n.1792G>T
|
|
|
ENST00000610370.2:n.3309G>T
|
|
|
ENST00000683058.1:n.1200G>T
|
|
|
ENST00000683722.1:c.1323G>T
|
ENSP00000507879.1:p.Glu441Asp
|
|
ENST00000684058.1:n.880G>T
|
|
|
ENST00000407796.7:c.1323G>T
|
ENSP00000384293.2:p.Glu441Asp
|
|
ENST00000649815.2:c.1323G>T
MANE Select
|
ENSP00000497822.1:p.Glu441Asp
|
|
ENST00000349310.7:c.1323G>T
|
ENSP00000270202.4:p.Glu441Asp
|
|
ENST00000402615.6:c.1323G>T
|
ENSP00000385326.2:p.Glu441Asp
|
|
ENST00000407796.6:c.1323G>T
|
ENSP00000384293.2:p.Glu441Asp
|
|
ENST00000544168.5:n.1258G>T
|
|
|
ENST00000553506.5:n.1721G>T
|
|
|
ENST00000554192.5:c.433G>T
|
|
|
ENST00000554581.5:c.1323G>T
|
ENSP00000451828.1:p.Glu441Asp
|
|
ENST00000554585.5:c.590G>T
|
ENSP00000481526.1:n.590G>T
|
|
ENST00000554848.5:c.1323G>T
|
ENSP00000451166.1:p.Glu441Asp
|
|
ENST00000555458.5:c.430G>T
|
|
|
ENST00000555528.5:c.1323G>T
|
ENSP00000450688.1:p.Glu441Asp
|
|
ENST00000557552.1:n.7287G>T
|
|
|
ENST00000610370.1:n.1754G>T
|
|
|
NM_001014431.1:c.1323G>T
|
NP_001014431.1:p.Glu441Asp
|
|
NM_001014432.1:c.1323G>T , LRG_721t1:c.1323G>T
|
NP_001014432.1:p.Glu441Asp
|
|
NM_005163.2:c.1323G>T , LRG_721t2:c.1323G>T
|
NP_005154.2:p.Glu441Asp
|
|
XM_005267401.1:c.1323G>T
|
XP_005267458.1:p.Glu441Asp
|
|
XM_011536543.1:c.1323G>T
|
XP_011534845.1:p.Glu441Asp
|
|
XR_002957536.1:n.3040G>T
|
|
|
NM_001014431.2:c.1323G>T
|
NP_001014431.1:p.Glu441Asp
|
|
NM_001014432.2:c.1323G>T
|
NP_001014432.1:p.Glu441Asp
|
|
NM_001382430.1:c.1323G>T
MANE Select
|
NP_001369359.1:p.Glu441Asp
|
|
NM_001382431.1:c.1323G>T
|
NP_001369360.1:p.Glu441Asp
|
|
NM_001382432.1:c.1323G>T
|
NP_001369361.1:p.Glu441Asp
|
|
NM_001382433.1:c.1323G>T
|
NP_001369362.1:p.Glu441Asp
|
|