|
ENST00000561667.2:c.*2782G>T
(FANCA)
|
ENSP00000512522.1:n.*2782G>T
|
|
|
ENST00000564475.6:c.4213G>T
(FANCA)
|
ENSP00000454977.2:p.Ala1405Ser
|
|
|
ENST00000567510.2:c.2783G>T
(FANCA)
|
ENSP00000455969.1:n.2783G>T
|
|
|
ENST00000568369.6:c.4213G>T
(FANCA)
|
ENSP00000456829.1:p.Ala1405Ser
|
|
|
ENST00000696274.1:n.4170G>T
(FANCA)
|
|
|
|
ENST00000696275.1:c.*3448G>T
(FANCA)
|
ENSP00000512517.1:n.*3448G>T
|
|
|
ENST00000696286.1:c.*122G>T
(FANCA)
|
ENSP00000512523.1:n.*122G>T
|
|
|
ENST00000696287.1:c.4084G>T
(FANCA)
|
ENSP00000512524.1:p.Ala1362Ser
|
|
|
ENST00000696291.1:c.*3641G>T
(FANCA)
|
ENSP00000512530.1:n.*3641G>T
|
|
|
ENST00000389301.8:c.4209G>T
(FANCA)
MANE Select
|
ENSP00000373952.3:p.Leu1403=
|
|
|
ENST00000443381.7:c.*687C>A
(ZNF276)
MANE Select
|
ENSP00000415836.2:n.*687C>A
|
|
|
ENST00000289816.9:c.*687C>A
(ZNF276)
|
ENSP00000289816.5:n.*687C>A
|
|
|
ENST00000389301.7:c.4209G>T
(FANCA)
|
ENSP00000373952.3:p.Leu1403=
|
|
|
ENST00000561722.5:c.436-7G>T
(FANCA)
|
ENSP00000456608.1:n.436-7G>T
|
|
|
ENST00000562424.1:n.480G>T
(FANCA)
|
|
|
|
ENST00000563983.5:n.2520C>A
(ZNF276)
|
|
|
|
ENST00000564475.5:c.543G>T
(FANCA)
|
|
|
|
ENST00000564870.1:c.410G>T
(FANCA)
|
|
|
|
ENST00000567879.5:c.583G>T
(FANCA)
|
ENSP00000457006.1:p.Ala195Ser
|
|
|
ENST00000568369.5:c.4213G>T
(FANCA)
|
ENSP00000456829.1:p.Ala1405Ser
|
|
|
NM_000135.2:c.4209G>T , LRG_495t1:c.4209G>T
(FANCA)
|
NP_000126.2:p.Leu1403=
|
|
|
NM_001113525.1:c.*687C>A
(ZNF276)
|
NP_001106997.1:n.*687C>A
|
|
|
NM_001286167.1:c.4213G>T
(FANCA)
|
NP_001273096.1:p.Ala1405Ser
|
|
|
NM_152287.3:c.*687C>A
(ZNF276)
|
NP_689500.2:n.*687C>A
|
|
|
NR_110122.1:n.2704C>A
(ZNF276)
|
|
|
|
NR_110126.1:n.2587C>A
(ZNF276)
|
|
|
|
NR_110128.1:n.2510C>A
(ZNF276)
|
|
|
|
NR_110129.1:n.2599C>A
(ZNF276)
|
|
|
|
XM_005256294.3:c.4213G>T
(FANCA)
|
XP_005256351.1:p.Ala1405Ser
|
|
|
XM_011522945.1:c.4084G>T
(FANCA)
|
XP_011521247.1:p.Ala1362Ser
|
|
|
XM_011522946.1:c.3190G>T
(FANCA)
|
XP_011521248.1:p.Ala1064Ser
|
|
|
XM_011522947.1:c.3190G>T
(FANCA)
|
XP_011521249.1:p.Ala1064Ser
|
|
|
XR_933244.1:n.4176G>T
(FANCA)
|
|
|
|
XR_933245.1:n.4113G>T
(FANCA)
|
|
|
|
NM_000135.3:c.4209G>T
(FANCA)
|
NP_000126.2:p.Leu1403=
|
|
|
NM_001286167.2:c.4213G>T
(FANCA)
|
NP_001273096.1:p.Ala1405Ser
|
|
|
XM_005256294.4:c.4213G>T
(FANCA)
|
XP_005256351.1:p.Ala1405Ser
|
|
|
XM_011522945.2:c.4084G>T
(FANCA)
|
XP_011521247.1:p.Ala1362Ser
|
|
|
XM_011522946.3:c.3190G>T
(FANCA)
|
XP_011521248.1:p.Ala1064Ser
|
|
|
XM_011522947.2:c.3190G>T
(FANCA)
|
XP_011521249.1:p.Ala1064Ser
|
|
|
XM_017023044.2:c.4080G>T
(FANCA)
|
XP_016878533.1:p.Leu1360=
|
|
|
XM_017023890.1:c.*687C>A
(ZNF276)
|
XP_016879379.1:n.*687C>A
|
|
|
XM_024450189.1:c.3190G>T
(FANCA)
|
XP_024305957.1:p.Ala1064Ser
|
|
|
XR_933244.2:n.4176G>T
(FANCA)
|
|
|
|
XR_933245.2:n.4113G>T
(FANCA)
|
|
|
|
XR_933484.2:n.2698C>A
(ZNF276)
|
|
|
|
NM_000135.4:c.4209G>T
(FANCA)
MANE Select
|
NP_000126.2:p.Leu1403=
|
|
|
NM_001113525.2:c.*687C>A
(ZNF276)
MANE Select
|
NP_001106997.1:n.*687C>A
|
|
|
NM_001286167.3:c.4213G>T
(FANCA)
|
NP_001273096.1:p.Ala1405Ser
|
|
|
NM_152287.4:c.*687C>A
(ZNF276)
|
NP_689500.2:n.*687C>A
|
|
|
NR_110122.2:n.2687C>A
(ZNF276)
|
|
|
|
NR_110126.2:n.2570C>A
(ZNF276)
|
|
|
|
NR_110129.2:n.2604C>A
(ZNF276)
|
|
|
|
NR_110128.2:n.2510C>A
(ZNF276)
|
|
|
