ENST00000508051.2:c.546C=
|
ENSP00000513677.1:p.Phe182=
|
|
ENST00000698351.1:c.864+513C=
|
ENSP00000513674.1:n.864+513C=
|
|
ENST00000698352.1:c.*929C=
|
ENSP00000513675.1:n.*929C=
|
|
ENST00000698353.1:n.1252C=
|
|
|
ENST00000698354.1:c.546C=
|
ENSP00000513676.1:p.Phe182=
|
|
ENST00000296795.8:c.1377C=
MANE Select
|
ENSP00000296795.3:p.Phe459=
|
|
ENST00000296795.7:c.1377C=
|
ENSP00000296795.2:p.Phe459=
|
|
ENST00000504367.1:c.546C=
|
ENSP00000423684.1:p.Phe182=
|
|
ENST00000512264.1:n.1453C=
|
|
|
NM_003265.2:c.1377C= , LRG_117t1:c.1377C=
|
NP_003256.1:p.Phe459=
|
|
NM_003265.3:c.1377C=
MANE Select
|
NP_003256.1:p.Phe459=
|
|