|
ENST00000561667.2:c.*2369G>A
(FANCA)
|
ENSP00000512522.1:n.*2369G>A
|
|
|
ENST00000564475.6:c.3891G>A
(FANCA)
|
ENSP00000454977.2:p.Lys1297=
|
|
|
ENST00000567510.2:c.2461G>A
(FANCA)
|
ENSP00000455969.1:n.2461G>A
|
|
|
ENST00000568369.6:c.3891G>A
(FANCA)
|
ENSP00000456829.1:p.Lys1297=
|
|
|
ENST00000696274.1:n.3852G>A
(FANCA)
|
|
|
|
ENST00000696275.1:c.*3126G>A
(FANCA)
|
ENSP00000512517.1:n.*3126G>A
|
|
|
ENST00000696286.1:c.3891G>A
(FANCA)
|
ENSP00000512523.1:p.Lys1297=
|
|
|
ENST00000696287.1:c.3762G>A
(FANCA)
|
ENSP00000512524.1:p.Lys1254=
|
|
|
ENST00000696291.1:c.*3323G>A
(FANCA)
|
ENSP00000512530.1:n.*3323G>A
|
|
|
ENST00000389301.8:c.3891G>A
(FANCA)
MANE Select
|
ENSP00000373952.3:p.Lys1297=
|
|
|
ENST00000443381.7:c.*1791C>T
(ZNF276)
MANE Select
|
ENSP00000415836.2:n.*1791C>T
|
|
|
ENST00000289816.9:c.*1791C>T
(ZNF276)
|
ENSP00000289816.5:n.*1791C>T
|
|
|
ENST00000305699.15:n.1134G>A
(FANCA)
|
|
|
|
ENST00000389301.7:c.3891G>A
(FANCA)
|
ENSP00000373952.3:p.Lys1297=
|
|
|
ENST00000561722.5:c.42G>A
(FANCA)
|
ENSP00000456608.1:p.Lys14=
|
|
|
ENST00000564475.5:c.221G>A
(FANCA)
|
|
|
|
ENST00000564870.1:c.92G>A
(FANCA)
|
|
|
|
ENST00000564969.5:n.176G>A
(FANCA)
|
|
|
|
ENST00000567879.5:c.369G>A
(FANCA)
|
ENSP00000457006.1:p.Lys123=
|
|
|
ENST00000568369.5:c.3891G>A
(FANCA)
|
ENSP00000456829.1:p.Lys1297=
|
|
|
ENST00000568626.1:c.600G>A
(FANCA)
|
|
|
|
NM_000135.2:c.3891G>A , LRG_495t1:c.3891G>A
(FANCA)
|
NP_000126.2:p.Lys1297=
|
|
|
NM_001113525.1:c.*1791C>T
(ZNF276)
|
NP_001106997.1:n.*1791C>T
|
|
|
NM_001286167.1:c.3891G>A
(FANCA)
|
NP_001273096.1:p.Lys1297=
|
|
|
NM_152287.3:c.*1791C>T
(ZNF276)
|
NP_689500.2:n.*1791C>T
|
|
|
XM_005256294.3:c.3891G>A
(FANCA)
|
XP_005256351.1:p.Lys1297=
|
|
|
XM_011522945.1:c.3762G>A
(FANCA)
|
XP_011521247.1:p.Lys1254=
|
|
|
XM_011522946.1:c.2868G>A
(FANCA)
|
XP_011521248.1:p.Lys956=
|
|
|
XM_011522947.1:c.2868G>A
(FANCA)
|
XP_011521249.1:p.Lys956=
|
|
|
XR_933244.1:n.3934G>A
(FANCA)
|
|
|
|
XR_933245.1:n.3795G>A
(FANCA)
|
|
|
|
NM_000135.3:c.3891G>A
(FANCA)
|
NP_000126.2:p.Lys1297=
|
|
|
NM_001286167.2:c.3891G>A
(FANCA)
|
NP_001273096.1:p.Lys1297=
|
|
|
XM_005256294.4:c.3891G>A
(FANCA)
|
XP_005256351.1:p.Lys1297=
|
|
|
XM_011522945.2:c.3762G>A
(FANCA)
|
XP_011521247.1:p.Lys1254=
|
|
|
XM_011522946.3:c.2868G>A
(FANCA)
|
XP_011521248.1:p.Lys956=
|
|
|
XM_011522947.2:c.2868G>A
(FANCA)
|
XP_011521249.1:p.Lys956=
|
|
|
XM_017023044.2:c.3762G>A
(FANCA)
|
XP_016878533.1:p.Lys1254=
|
|
|
XM_024450189.1:c.2868G>A
(FANCA)
|
XP_024305957.1:p.Lys956=
|
|
|
XR_001751866.1:n.3761G>A
(FANCA)
|
|
|
|
XR_933244.2:n.3934G>A
(FANCA)
|
|
|
|
XR_933245.2:n.3795G>A
(FANCA)
|
|
|
|
NM_000135.4:c.3891G>A
(FANCA)
MANE Select
|
NP_000126.2:p.Lys1297=
|
|
|
NM_001113525.2:c.*1791C>T
(ZNF276)
MANE Select
|
NP_001106997.1:n.*1791C>T
|
|
|
NM_001286167.3:c.3891G>A
(FANCA)
|
NP_001273096.1:p.Lys1297=
|
|
|
NM_152287.4:c.*1791C>T
(ZNF276)
|
NP_689500.2:n.*1791C>T
|
|
|
NR_110122.2:n.3791C>T
(ZNF276)
|
|
|
|
NR_110126.2:n.3674C>T
(ZNF276)
|
|
|
|
NR_110129.2:n.3708C>T
(ZNF276)
|
|
|
|
NR_110128.2:n.3614C>T
(ZNF276)
|
|
|
