ENST00000406938.3:c.456A>T
(CHKB)
MANE Select
|
ENSP00000384400.3:p.Pro152=
|
|
ENST00000406938.2:c.456A>T
(CHKB)
|
ENSP00000384400.2:p.Pro152=
|
|
ENST00000463053.1:n.605A>T
(CHKB)
|
|
|
ENST00000468532.5:n.333A>T
(CHKB)
|
|
|
ENST00000476289.5:n.729A>T
(CHKB)
|
|
|
ENST00000479003.5:n.1081A>T
(CHKB)
|
|
|
ENST00000481673.5:n.906A>T
(CHKB)
|
|
|
ENST00000484266.5:n.576+704A>T
(CHKB)
|
|
|
ENST00000492556.5:n.1226A>T
(CHKB-CPT1B)
|
|
|
ENST00000492582.5:n.1115A>T
(CHKB)
|
|
|
NM_005198.4:c.456A>T , LRG_855t1:c.456A>T
(CHKB)
|
NP_005189.2:p.Pro152=
|
|
NR_027928.2:n.674A>T
(CHKB-CPT1B)
|
|
|
NM_005198.5:c.456A>T
(CHKB)
MANE Select
|
NP_005189.2:p.Pro152=
|
|