ENST00000480188.2:n.1390T>C
|
|
|
ENST00000696279.1:c.4676T>C
|
|
|
ENST00000696280.1:n.4445T>C
|
|
|
ENST00000696281.1:c.4374T>C
|
ENSP00000512521.1:p.Asp1458=
|
|
ENST00000697921.1:n.3234T>C
|
|
|
ENST00000697922.1:c.*4346T>C
|
ENSP00000513478.1:n.*4346T>C
|
|
ENST00000697923.1:n.4801T>C
|
|
|
ENST00000223642.3:c.4356T>C
MANE Select
|
ENSP00000223642.1:p.Asp1452=
|
|
ENST00000223642.2:c.4356T>C
|
ENSP00000223642.1:p.Asp1452=
|
|
NM_001735.2:c.4356T>C , LRG_28t1:c.4356T>C
|
NP_001726.2:p.Asp1452=
|
|
XM_011518980.1:c.4371T>C
|
XP_011517282.1:p.Asp1457=
|
|
NM_001317163.1:c.4374T>C
|
NP_001304092.1:p.Asp1458=
|
|
NM_001317163.2:c.4374T>C
|
NP_001304092.1:p.Asp1458=
|
|
NM_001735.3:c.4356T>C
MANE Select
|
NP_001726.2:p.Asp1452=
|
|