NM_003265.3:c.1234C=
MANE Select
|
NP_003256.1:p.Leu412=
|
ENST00000296795.8:c.1234C=
MANE Select
|
ENSP00000296795.3:p.Leu412=
|
NM_003265.2:c.1234C= , LRG_117t1:c.1234C=
|
NP_003256.1:p.Leu412=
|
ENST00000296795.7:c.1234C=
|
ENSP00000296795.2:p.Leu412=
|
ENST00000504367.1:c.403C=
|
ENSP00000423684.1:p.Leu135=
|
ENST00000508051.2:c.403C=
|
ENSP00000513677.1:p.Leu135=
|
ENST00000512264.1:n.1310C=
|
|
ENST00000513189.1:c.1042C=
|
ENSP00000423386.1:p.Leu348=
|
ENST00000698351.1:c.864+370C=
|
ENSP00000513674.1:n.864+370C=
|
ENST00000698352.1:c.*786C=
|
ENSP00000513675.1:n.*786C=
|
ENST00000698353.1:n.1109C=
|
|
ENST00000698354.1:c.403C=
|
ENSP00000513676.1:p.Leu135=
|