|
ENST00000406938.3:c.708C>T
(CHKB)
MANE Select
|
ENSP00000384400.3:p.Val236=
|
|
|
ENST00000406938.2:c.708C>T
(CHKB)
|
ENSP00000384400.2:p.Val236=
|
|
|
ENST00000463053.1:n.857C>T
(CHKB)
|
|
|
|
ENST00000468532.5:n.585C>T
(CHKB)
|
|
|
|
ENST00000471515.5:n.70C>T
(CHKB)
|
|
|
|
ENST00000476289.5:n.981C>T
(CHKB)
|
|
|
|
ENST00000479003.5:n.1333C>T
(CHKB)
|
|
|
|
ENST00000481673.5:n.1158C>T
(CHKB)
|
|
|
|
ENST00000484266.5:n.703C>T
(CHKB)
|
|
|
|
ENST00000489453.1:n.247C>T
(CHKB)
|
|
|
|
ENST00000492556.5:n.1478C>T
(CHKB-CPT1B)
|
|
|
|
ENST00000492582.5:n.1367C>T
(CHKB)
|
|
|
|
NM_005198.4:c.708C>T , LRG_855t1:c.708C>T
(CHKB)
|
NP_005189.2:p.Val236=
|
|
|
NR_027928.2:n.926C>T
(CHKB-CPT1B)
|
|
|
|
NM_005198.5:c.708C>T
(CHKB)
MANE Select
|
NP_005189.2:p.Val236=
|
|
