ENST00000426263.10:c.399C=
MANE Select
|
ENSP00000416293.2:p.Cys133=
|
|
ENST00000674765.1:c.399C=
|
ENSP00000501811.1:p.Cys133=
|
|
ENST00000675112.1:n.422C=
|
|
|
ENST00000676254.1:n.848C=
|
|
|
ENST00000372500.4:c.303C=
|
ENSP00000361578.4:p.Cys101=
|
|
ENST00000426263.7:c.399C=
|
ENSP00000416293.2:p.Cys133=
|
|
ENST00000439722.2:c.278C=
|
ENSP00000395521.2:n.278C=
|
|
ENST00000475162.3:c.298C=
|
|
|
ENST00000625233.2:n.607C=
|
|
|
ENST00000630287.2:c.399C=
|
ENSP00000486694.1:p.Cys133=
|
|
NM_006516.2:c.399C=
|
NP_006507.2:p.Cys133=
|
|
NM_006516.3:c.399C=
|
NP_006507.2:p.Cys133=
|
|
NM_006516.4:c.399C=
MANE Select
|
NP_006507.2:p.Cys133=
|
|