ENST00000492653.6:c.*236T>A
|
ENSP00000515192.1:n.*236T>A
|
|
ENST00000703133.1:c.*1186T>A
|
ENSP00000515188.1:n.*1186T>A
|
|
ENST00000703136.1:c.*570T>A
|
ENSP00000515190.1:n.*570T>A
|
|
ENST00000374839.8:c.612T>A
MANE Select
|
ENSP00000363972.3:p.Pro204=
|
|
ENST00000337990.2:c.543T>A
|
ENSP00000338650.2:p.Pro181=
|
|
ENST00000374839.7:c.612T>A
|
ENSP00000363972.3:p.Pro204=
|
|
ENST00000447788.6:c.449T>A
|
ENSP00000399126.2:p.Leu150His
|
|
ENST00000488406.1:n.132T>A
|
|
|
ENST00000488608.5:n.2789T>A
|
|
|
ENST00000488831.5:n.600T>A
|
|
|
ENST00000492653.5:n.740T>A
|
|
|
NM_001178032.2:c.543T>A
|
NP_001171503.1:p.Pro181=
|
|
NM_001178033.2:c.449T>A
|
NP_001171504.1:p.Leu150His
|
|
NM_001243804.1:c.543T>A
|
NP_001230733.1:p.Pro181=
|
|
NM_018684.3:c.612T>A
|
NP_061154.1:p.Pro204=
|
|
NR_045044.1:n.1023T>A
|
|
|
NM_018684.4:c.612T>A
MANE Select
|
NP_061154.1:p.Pro204=
|
|
NM_001178032.3:c.543T>A
|
NP_001171503.1:p.Pro181=
|
|
NM_001243804.2:c.543T>A
|
NP_001230733.1:p.Pro181=
|
|
NR_045044.2:n.940T>A
|
|
|
NM_001178033.3:c.449T>A
|
NP_001171504.1:p.Leu150His
|
|