|
ENST00000561667.2:c.*2755A>T
(FANCA)
|
ENSP00000512522.1:n.*2755A>T
|
|
|
ENST00000564475.6:c.4186A>T
(FANCA)
|
ENSP00000454977.2:p.Thr1396Ser
|
|
|
ENST00000567510.2:c.2756A>T
(FANCA)
|
ENSP00000455969.1:n.2756A>T
|
|
|
ENST00000568369.6:c.4186A>T
(FANCA)
|
ENSP00000456829.1:p.Thr1396Ser
|
|
|
ENST00000696274.1:n.4143A>T
(FANCA)
|
|
|
|
ENST00000696275.1:c.*3421A>T
(FANCA)
|
ENSP00000512517.1:n.*3421A>T
|
|
|
ENST00000696286.1:c.*95A>T
(FANCA)
|
ENSP00000512523.1:n.*95A>T
|
|
|
ENST00000696287.1:c.4057A>T
(FANCA)
|
ENSP00000512524.1:p.Thr1353Ser
|
|
|
ENST00000696291.1:c.*3614A>T
(FANCA)
|
ENSP00000512530.1:n.*3614A>T
|
|
|
ENST00000389301.8:c.4182A>T
(FANCA)
MANE Select
|
ENSP00000373952.3:p.Glu1394Asp
|
|
|
ENST00000443381.7:c.*714T>A
(ZNF276)
MANE Select
|
ENSP00000415836.2:n.*714T>A
|
|
|
ENST00000289816.9:c.*714T>A
(ZNF276)
|
ENSP00000289816.5:n.*714T>A
|
|
|
ENST00000389301.7:c.4182A>T
(FANCA)
|
ENSP00000373952.3:p.Glu1394Asp
|
|
|
ENST00000561722.5:c.436-34A>T
(FANCA)
|
ENSP00000456608.1:n.436-34A>T
|
|
|
ENST00000562424.1:n.453A>T
(FANCA)
|
|
|
|
ENST00000563983.5:n.2547T>A
(ZNF276)
|
|
|
|
ENST00000564475.5:c.516A>T
(FANCA)
|
|
|
|
ENST00000564870.1:c.383A>T
(FANCA)
|
|
|
|
ENST00000567879.5:c.556A>T
(FANCA)
|
ENSP00000457006.1:p.Thr186Ser
|
|
|
ENST00000568369.5:c.4186A>T
(FANCA)
|
ENSP00000456829.1:p.Thr1396Ser
|
|
|
NM_000135.2:c.4182A>T , LRG_495t1:c.4182A>T
(FANCA)
|
NP_000126.2:p.Glu1394Asp
|
|
|
NM_001113525.1:c.*714T>A
(ZNF276)
|
NP_001106997.1:n.*714T>A
|
|
|
NM_001286167.1:c.4186A>T
(FANCA)
|
NP_001273096.1:p.Thr1396Ser
|
|
|
NM_152287.3:c.*714T>A
(ZNF276)
|
NP_689500.2:n.*714T>A
|
|
|
NR_110122.1:n.2731T>A
(ZNF276)
|
|
|
|
NR_110126.1:n.2614T>A
(ZNF276)
|
|
|
|
NR_110128.1:n.2537T>A
(ZNF276)
|
|
|
|
NR_110129.1:n.2626T>A
(ZNF276)
|
|
|
|
XM_005256294.3:c.4186A>T
(FANCA)
|
XP_005256351.1:p.Thr1396Ser
|
|
|
XM_011522945.1:c.4057A>T
(FANCA)
|
XP_011521247.1:p.Thr1353Ser
|
|
|
XM_011522946.1:c.3163A>T
(FANCA)
|
XP_011521248.1:p.Thr1055Ser
|
|
|
XM_011522947.1:c.3163A>T
(FANCA)
|
XP_011521249.1:p.Thr1055Ser
|
|
|
XR_933244.1:n.4149A>T
(FANCA)
|
|
|
|
XR_933245.1:n.4086A>T
(FANCA)
|
|
|
|
NM_000135.3:c.4182A>T
(FANCA)
|
NP_000126.2:p.Glu1394Asp
|
|
|
NM_001286167.2:c.4186A>T
(FANCA)
|
NP_001273096.1:p.Thr1396Ser
|
|
|
XM_005256294.4:c.4186A>T
(FANCA)
|
XP_005256351.1:p.Thr1396Ser
|
|
|
XM_011522945.2:c.4057A>T
(FANCA)
|
XP_011521247.1:p.Thr1353Ser
|
|
|
XM_011522946.3:c.3163A>T
(FANCA)
|
XP_011521248.1:p.Thr1055Ser
|
|
|
XM_011522947.2:c.3163A>T
(FANCA)
|
XP_011521249.1:p.Thr1055Ser
|
|
|
XM_017023044.2:c.4053A>T
(FANCA)
|
XP_016878533.1:p.Glu1351Asp
|
|
|
XM_017023890.1:c.*714T>A
(ZNF276)
|
XP_016879379.1:n.*714T>A
|
|
|
XM_024450189.1:c.3163A>T
(FANCA)
|
XP_024305957.1:p.Thr1055Ser
|
|
|
XR_933244.2:n.4149A>T
(FANCA)
|
|
|
|
XR_933245.2:n.4086A>T
(FANCA)
|
|
|
|
XR_933484.2:n.2725T>A
(ZNF276)
|
|
|
|
NM_000135.4:c.4182A>T
(FANCA)
MANE Select
|
NP_000126.2:p.Glu1394Asp
|
|
|
NM_001113525.2:c.*714T>A
(ZNF276)
MANE Select
|
NP_001106997.1:n.*714T>A
|
|
|
NM_001286167.3:c.4186A>T
(FANCA)
|
NP_001273096.1:p.Thr1396Ser
|
|
|
NM_152287.4:c.*714T>A
(ZNF276)
|
NP_689500.2:n.*714T>A
|
|
|
NR_110122.2:n.2714T>A
(ZNF276)
|
|
|
|
NR_110126.2:n.2597T>A
(ZNF276)
|
|
|
|
NR_110129.2:n.2631T>A
(ZNF276)
|
|
|
|
NR_110128.2:n.2537T>A
(ZNF276)
|
|
|
