ENST00000381375.7:c.126+1895G=
(CDC20B)
MANE Select
|
ENSP00000370781.2:n.126+1895G=
|
|
ENST00000296733.5:c.126+1895G=
(CDC20B)
|
ENSP00000296733.1:n.126+1895G=
|
|
ENST00000322374.10:c.126+1895G=
(CDC20B)
|
ENSP00000315720.6:n.126+1895G=
|
|
ENST00000381375.6:c.126+1895G=
(CDC20B)
|
ENSP00000370781.2:n.126+1895G=
|
|
ENST00000507931.1:c.63+2245G=
(CDC20B)
|
ENSP00000423919.1:n.63+2245G=
|
|
ENST00000513180.5:c.126+1895G=
(CDC20B)
|
ENSP00000426776.1:n.126+1895G=
|
|
NM_001145734.2:c.126+1895G=
(CDC20B)
|
NP_001139206.2:n.126+1895G=
|
|
NM_001170402.1:c.126+1895G=
(CDC20B)
MANE Select
|
NP_001163873.1:n.126+1895G=
|
|
NM_152623.2:c.126+1895G=
(CDC20B)
|
NP_689836.2:n.126+1895G=
|
|
NR_030387.1:n.50G=
(MIR449B)
|
|
|
XM_011543218.1:c.126+1895G=
(CDC20B)
|
XP_011541520.1:n.126+1895G=
|
|
XM_011543218.2:c.126+1895G=
(CDC20B)
|
XP_011541520.1:n.126+1895G=
|
|