|
ENST00000561667.2:c.*2834G>A
(FANCA)
|
ENSP00000512522.1:n.*2834G>A
|
|
|
ENST00000564475.6:c.4265G>A
(FANCA)
|
ENSP00000454977.2:p.Gly1422Asp
|
|
|
ENST00000567510.2:c.2834+1G>A
(FANCA)
|
ENSP00000455969.1:n.2834+1G>A
|
|
|
ENST00000568369.6:c.4264+1G>A
(FANCA)
|
ENSP00000456829.1:n.4264+1G>A
|
|
|
ENST00000696274.1:n.4222G>A
(FANCA)
|
|
|
|
ENST00000696275.1:c.*3500G>A
(FANCA)
|
ENSP00000512517.1:n.*3500G>A
|
|
|
ENST00000696286.1:c.*173+1G>A
(FANCA)
|
ENSP00000512523.1:n.*173+1G>A
|
|
|
ENST00000696287.1:c.4136G>A
(FANCA)
|
ENSP00000512524.1:p.Gly1379Asp
|
|
|
ENST00000696291.1:c.*3693G>A
(FANCA)
|
ENSP00000512530.1:n.*3693G>A
|
|
|
ENST00000389301.8:c.4260+1G>A
(FANCA)
MANE Select
|
ENSP00000373952.3:n.4260+1G>A
|
|
|
ENST00000443381.7:c.*635C>T
(ZNF276)
MANE Select
|
ENSP00000415836.2:n.*635C>T
|
|
|
ENST00000289816.9:c.*635C>T
(ZNF276)
|
ENSP00000289816.5:n.*635C>T
|
|
|
ENST00000389301.7:c.4260+1G>A
(FANCA)
|
ENSP00000373952.3:n.4260+1G>A
|
|
|
ENST00000561722.5:c.480+1G>A
(FANCA)
|
ENSP00000456608.1:n.480+1G>A
|
|
|
ENST00000562424.1:n.531+1G>A
(FANCA)
|
|
|
|
ENST00000563983.5:n.2468C>T
(ZNF276)
|
|
|
|
ENST00000564475.5:c.595G>A
(FANCA)
|
|
|
|
ENST00000567879.5:c.634+1G>A
(FANCA)
|
ENSP00000457006.1:n.634+1G>A
|
|
|
ENST00000568369.5:c.4264+1G>A
(FANCA)
|
ENSP00000456829.1:n.4264+1G>A
|
|
|
NM_000135.2:c.4260+1G>A , LRG_495t1:c.4260+1G>A
(FANCA)
|
NP_000126.2:n.4260+1G>A
|
|
|
NM_001113525.1:c.*635C>T
(ZNF276)
|
NP_001106997.1:n.*635C>T
|
|
|
NM_001286167.1:c.4264+1G>A
(FANCA)
|
NP_001273096.1:n.4264+1G>A
|
|
|
NM_152287.3:c.*635C>T
(ZNF276)
|
NP_689500.2:n.*635C>T
|
|
|
NR_110122.1:n.2652C>T
(ZNF276)
|
|
|
|
NR_110126.1:n.2535C>T
(ZNF276)
|
|
|
|
NR_110128.1:n.2458C>T
(ZNF276)
|
|
|
|
NR_110129.1:n.2547C>T
(ZNF276)
|
|
|
|
XM_005256294.3:c.4265G>A
(FANCA)
|
XP_005256351.1:p.Gly1422Asp
|
|
|
XM_011522945.1:c.4136G>A
(FANCA)
|
XP_011521247.1:p.Gly1379Asp
|
|
|
XM_011522946.1:c.3242G>A
(FANCA)
|
XP_011521248.1:p.Gly1081Asp
|
|
|
XM_011522947.1:c.3242G>A
(FANCA)
|
XP_011521249.1:p.Gly1081Asp
|
|
|
XR_933244.1:n.4227+1G>A
(FANCA)
|
|
|
|
XR_933245.1:n.4164+1G>A
(FANCA)
|
|
|
|
NM_000135.3:c.4260+1G>A
(FANCA)
|
NP_000126.2:n.4260+1G>A
|
|
|
NM_001286167.2:c.4264+1G>A
(FANCA)
|
NP_001273096.1:n.4264+1G>A
|
|
|
XM_005256294.4:c.4265G>A
(FANCA)
|
XP_005256351.1:p.Gly1422Asp
|
|
|
XM_011522945.2:c.4136G>A
(FANCA)
|
XP_011521247.1:p.Gly1379Asp
|
|
|
XM_011522946.3:c.3242G>A
(FANCA)
|
XP_011521248.1:p.Gly1081Asp
|
|
|
XM_011522947.2:c.3242G>A
(FANCA)
|
XP_011521249.1:p.Gly1081Asp
|
|
|
XM_017023044.2:c.4131+1G>A
(FANCA)
|
XP_016878533.1:n.4131+1G>A
|
|
|
XM_017023890.1:c.*635C>T
(ZNF276)
|
XP_016879379.1:n.*635C>T
|
|
|
XM_024450189.1:c.3242G>A
(FANCA)
|
XP_024305957.1:p.Gly1081Asp
|
|
|
XR_933244.2:n.4227+1G>A
(FANCA)
|
|
|
|
XR_933245.2:n.4164+1G>A
(FANCA)
|
|
|
|
XR_933484.2:n.2646C>T
(ZNF276)
|
|
|
|
NM_000135.4:c.4260+1G>A
(FANCA)
MANE Select
|
NP_000126.2:n.4260+1G>A
|
|
|
NM_001113525.2:c.*635C>T
(ZNF276)
MANE Select
|
NP_001106997.1:n.*635C>T
|
|
|
NM_001286167.3:c.4264+1G>A
(FANCA)
|
NP_001273096.1:n.4264+1G>A
|
|
|
NM_152287.4:c.*635C>T
(ZNF276)
|
NP_689500.2:n.*635C>T
|
|
|
NR_110122.2:n.2635C>T
(ZNF276)
|
|
|
|
NR_110126.2:n.2518C>T
(ZNF276)
|
|
|
|
NR_110129.2:n.2552C>T
(ZNF276)
|
|
|
|
NR_110128.2:n.2458C>T
(ZNF276)
|
|
|
