ENST00000406938.3:c.333+112A>G
(CHKB)
MANE Select
|
ENSP00000384400.3:n.333+112A>G
|
|
ENST00000406938.2:c.333+112A>G
(CHKB)
|
ENSP00000384400.2:n.333+112A>G
|
|
ENST00000463053.1:n.416-42A>G
(CHKB)
|
|
|
ENST00000465842.1:n.172+112A>G
(CHKB)
|
|
|
ENST00000468532.5:n.210+112A>G
(CHKB)
|
|
|
ENST00000476289.5:n.606+112A>G
(CHKB)
|
|
|
ENST00000479003.5:n.684A>G
(CHKB)
|
|
|
ENST00000481673.5:n.509A>G
(CHKB)
|
|
|
ENST00000484266.5:n.576+112A>G
(CHKB)
|
|
|
ENST00000492556.5:n.829A>G
(CHKB-CPT1B)
|
|
|
ENST00000492582.5:n.718A>G
(CHKB)
|
|
|
NM_005198.4:c.333+112A>G , LRG_855t1:c.333+112A>G
(CHKB)
|
NP_005189.2:n.333+112A>G
|
|
NR_027928.2:n.551+112A>G
(CHKB-CPT1B)
|
|
|
NM_005198.5:c.333+112A>G
(CHKB)
MANE Select
|
NP_005189.2:n.333+112A>G
|
|