ENST00000480188.2:n.1446A>T
|
|
|
ENST00000696279.1:c.4732A>T
|
|
|
ENST00000696280.1:n.4501A>T
|
|
|
ENST00000696281.1:c.4430A>T
|
ENSP00000512521.1:p.Asp1477Val
|
|
ENST00000697921.1:n.3290A>T
|
|
|
ENST00000697922.1:c.*4402A>T
|
ENSP00000513478.1:n.*4402A>T
|
|
ENST00000697923.1:n.4857A>T
|
|
|
ENST00000223642.3:c.4412A>T
MANE Select
|
ENSP00000223642.1:p.Asp1471Val
|
|
ENST00000223642.2:c.4412A>T
|
ENSP00000223642.1:p.Asp1471Val
|
|
NM_001735.2:c.4412A>T , LRG_28t1:c.4412A>T
|
NP_001726.2:p.Asp1471Val
|
|
XM_011518980.1:c.4427A>T
|
XP_011517282.1:p.Asp1476Val
|
|
NM_001317163.1:c.4430A>T
|
NP_001304092.1:p.Asp1477Val
|
|
NM_001317163.2:c.4430A>T
|
NP_001304092.1:p.Asp1477Val
|
|
NM_001735.3:c.4412A>T
MANE Select
|
NP_001726.2:p.Asp1471Val
|
|