ENST00000476032.2:c.124G>T
|
ENSP00000515193.1:p.Glu42Ter
|
|
ENST00000492653.6:c.193G>T
|
ENSP00000515192.1:p.Glu65Ter
|
|
ENST00000703133.1:c.*767G>T
|
ENSP00000515188.1:n.*767G>T
|
|
ENST00000703136.1:c.*151G>T
|
ENSP00000515190.1:n.*151G>T
|
|
ENST00000374839.8:c.193G>T
MANE Select
|
ENSP00000363972.3:p.Glu65Ter
|
|
ENST00000337990.2:c.124G>T
|
ENSP00000338650.2:p.Glu42Ter
|
|
ENST00000374839.7:c.193G>T
|
ENSP00000363972.3:p.Glu65Ter
|
|
ENST00000447788.6:c.193G>T
|
ENSP00000399126.2:p.Glu65Ter
|
|
ENST00000476032.1:n.434G>T
|
|
|
ENST00000488608.5:n.349G>T
|
|
|
ENST00000488831.5:n.181G>T
|
|
|
ENST00000492653.5:n.289G>T
|
|
|
NM_001178032.2:c.124G>T
|
NP_001171503.1:p.Glu42Ter
|
|
NM_001178033.2:c.193G>T
|
NP_001171504.1:p.Glu65Ter
|
|
NM_001243804.1:c.124G>T
|
NP_001230733.1:p.Glu42Ter
|
|
NM_018684.3:c.193G>T
|
NP_061154.1:p.Glu65Ter
|
|
NR_045044.1:n.604G>T
|
|
|
NM_018684.4:c.193G>T
MANE Select
|
NP_061154.1:p.Glu65Ter
|
|
NM_001178032.3:c.124G>T
|
NP_001171503.1:p.Glu42Ter
|
|
NM_001243804.2:c.124G>T
|
NP_001230733.1:p.Glu42Ter
|
|
NR_045044.2:n.521G>T
|
|
|
NM_001178033.3:c.193G>T
|
NP_001171504.1:p.Glu65Ter
|
|