ENST00000480188.2:n.1413T>A
|
|
|
ENST00000696279.1:c.4699T>A
|
|
|
ENST00000696280.1:n.4468T>A
|
|
|
ENST00000696281.1:c.4397T>A
|
ENSP00000512521.1:p.Val1466Asp
|
|
ENST00000697921.1:n.3257T>A
|
|
|
ENST00000697922.1:c.*4369T>A
|
ENSP00000513478.1:n.*4369T>A
|
|
ENST00000697923.1:n.4824T>A
|
|
|
ENST00000223642.3:c.4379T>A
MANE Select
|
ENSP00000223642.1:p.Val1460Asp
|
|
ENST00000223642.2:c.4379T>A
|
ENSP00000223642.1:p.Val1460Asp
|
|
NM_001735.2:c.4379T>A , LRG_28t1:c.4379T>A
|
NP_001726.2:p.Val1460Asp
|
|
XM_011518980.1:c.4394T>A
|
XP_011517282.1:p.Val1465Asp
|
|
NM_001317163.1:c.4397T>A
|
NP_001304092.1:p.Val1466Asp
|
|
NM_001317163.2:c.4397T>A
|
NP_001304092.1:p.Val1466Asp
|
|
NM_001735.3:c.4379T>A
MANE Select
|
NP_001726.2:p.Val1460Asp
|
|