ENST00000476032.2:c.113C>T
|
ENSP00000515193.1:p.Ala38Val
|
|
ENST00000492653.6:c.182C>T
|
ENSP00000515192.1:p.Ala61Val
|
|
ENST00000703133.1:c.*756C>T
|
ENSP00000515188.1:n.*756C>T
|
|
ENST00000703136.1:c.*140C>T
|
ENSP00000515190.1:n.*140C>T
|
|
ENST00000374839.8:c.182C>T
MANE Select
|
ENSP00000363972.3:p.Ala61Val
|
|
ENST00000337990.2:c.113C>T
|
ENSP00000338650.2:p.Ala38Val
|
|
ENST00000374839.7:c.182C>T
|
ENSP00000363972.3:p.Ala61Val
|
|
ENST00000447788.6:c.182C>T
|
ENSP00000399126.2:p.Ala61Val
|
|
ENST00000476032.1:n.423C>T
|
|
|
ENST00000488608.5:n.338C>T
|
|
|
ENST00000488831.5:n.170C>T
|
|
|
ENST00000492653.5:n.278C>T
|
|
|
NM_001178032.2:c.113C>T
|
NP_001171503.1:p.Ala38Val
|
|
NM_001178033.2:c.182C>T
|
NP_001171504.1:p.Ala61Val
|
|
NM_001243804.1:c.113C>T
|
NP_001230733.1:p.Ala38Val
|
|
NM_018684.3:c.182C>T
|
NP_061154.1:p.Ala61Val
|
|
NR_045044.1:n.593C>T
|
|
|
NM_018684.4:c.182C>T
MANE Select
|
NP_061154.1:p.Ala61Val
|
|
NM_001178032.3:c.113C>T
|
NP_001171503.1:p.Ala38Val
|
|
NM_001243804.2:c.113C>T
|
NP_001230733.1:p.Ala38Val
|
|
NR_045044.2:n.510C>T
|
|
|
NM_001178033.3:c.182C>T
|
NP_001171504.1:p.Ala61Val
|
|