ENST00000480188.2:n.1468G>T
|
|
|
ENST00000696279.1:c.4754G>T
|
|
|
ENST00000696280.1:n.4523G>T
|
|
|
ENST00000696281.1:c.4452G>T
|
ENSP00000512521.1:p.Arg1484=
|
|
ENST00000697921.1:n.3312G>T
|
|
|
ENST00000697922.1:c.*4424G>T
|
ENSP00000513478.1:n.*4424G>T
|
|
ENST00000697923.1:n.4879G>T
|
|
|
ENST00000223642.3:c.4434G>T
MANE Select
|
ENSP00000223642.1:p.Arg1478=
|
|
ENST00000223642.2:c.4434G>T
|
ENSP00000223642.1:p.Arg1478=
|
|
NM_001735.2:c.4434G>T , LRG_28t1:c.4434G>T
|
NP_001726.2:p.Arg1478=
|
|
XM_011518980.1:c.4449G>T
|
XP_011517282.1:p.Arg1483=
|
|
NM_001317163.1:c.4452G>T
|
NP_001304092.1:p.Arg1484=
|
|
NM_001317163.2:c.4452G>T
|
NP_001304092.1:p.Arg1484=
|
|
NM_001735.3:c.4434G>T
MANE Select
|
NP_001726.2:p.Arg1478=
|
|