ENST00000480188.2:n.1199T>A
|
|
|
ENST00000696279.1:c.4485T>A
|
|
|
ENST00000696280.1:n.4254T>A
|
|
|
ENST00000696281.1:c.4183T>A
|
ENSP00000512521.1:p.Ser1395Thr
|
|
ENST00000697921.1:n.3043T>A
|
|
|
ENST00000697922.1:c.*4155T>A
|
ENSP00000513478.1:n.*4155T>A
|
|
ENST00000697923.1:n.4610T>A
|
|
|
ENST00000223642.3:c.4165T>A
MANE Select
|
ENSP00000223642.1:p.Ser1389Thr
|
|
ENST00000223642.2:c.4165T>A
|
ENSP00000223642.1:p.Ser1389Thr
|
|
NM_001735.2:c.4165T>A , LRG_28t1:c.4165T>A
|
NP_001726.2:p.Ser1389Thr
|
|
XM_011518980.1:c.4180T>A
|
XP_011517282.1:p.Ser1394Thr
|
|
NM_001317163.1:c.4183T>A
|
NP_001304092.1:p.Ser1395Thr
|
|
NM_001317163.2:c.4183T>A
|
NP_001304092.1:p.Ser1395Thr
|
|
NM_001735.3:c.4165T>A
MANE Select
|
NP_001726.2:p.Ser1389Thr
|
|