ENST00000355832.10:c.3634T=
MANE Select
|
ENSP00000348089.5:p.Cys1212=
|
|
ENST00000679552.1:n.705T=
|
|
|
ENST00000679871.1:n.780T=
|
|
|
ENST00000679974.1:n.683T=
|
|
|
ENST00000681632.1:n.5037T=
|
|
|
ENST00000681659.1:c.3475T=
|
ENSP00000505631.1:p.Cys1159=
|
|
ENST00000355832.9:c.3634T=
|
ENSP00000348089.5:p.Cys1212=
|
|
ENST00000623073.3:c.*1930T=
|
ENSP00000485650.1:n.*1930T=
|
|
ENST00000623115.3:c.1744T=
|
ENSP00000485321.1:p.Cys582=
|
|
ENST00000624341.3:c.1466T=
|
|
|
NM_000124.3:c.3634T=
|
NP_000115.1:p.Cys1212=
|
|
XR_945953.1:n.243-1239A=
|
|
|
NM_001346440.1:c.3634T=
|
NP_001333369.1:p.Cys1212=
|
|
NM_000124.4:c.3634T=
MANE Select
|
NP_000115.1:p.Cys1212=
|
|
NM_001346440.2:c.3634T=
|
NP_001333369.1:p.Cys1212=
|
|