|
ENST00000561667.2:c.*2306+2T>A
(FANCA)
|
ENSP00000512522.1:n.*2306+2T>A
|
|
|
ENST00000564475.6:c.3828+2T>A
(FANCA)
|
ENSP00000454977.2:n.3828+2T>A
|
|
|
ENST00000567510.2:c.2398+2T>A
(FANCA)
|
ENSP00000455969.1:n.2398+2T>A
|
|
|
ENST00000568369.6:c.3828+2T>A
(FANCA)
|
ENSP00000456829.1:n.3828+2T>A
|
|
|
ENST00000696274.1:n.3789+2T>A
(FANCA)
|
|
|
|
ENST00000696275.1:c.*3063+2T>A
(FANCA)
|
ENSP00000512517.1:n.*3063+2T>A
|
|
|
ENST00000696286.1:c.3828+2T>A
(FANCA)
|
ENSP00000512523.1:n.3828+2T>A
|
|
|
ENST00000696287.1:c.3699+2T>A
(FANCA)
|
ENSP00000512524.1:n.3699+2T>A
|
|
|
ENST00000696291.1:c.*3260+2T>A
(FANCA)
|
ENSP00000512530.1:n.*3260+2T>A
|
|
|
ENST00000389301.8:c.3828+2T>A
(FANCA)
MANE Select
|
ENSP00000373952.3:n.3828+2T>A
|
|
|
ENST00000443381.7:c.*2556A>T
(ZNF276)
MANE Select
|
ENSP00000415836.2:n.*2556A>T
|
|
|
ENST00000289816.9:c.*2556A>T
(ZNF276)
|
ENSP00000289816.5:n.*2556A>T
|
|
|
ENST00000305699.15:n.1071+2T>A
(FANCA)
|
|
|
|
ENST00000389301.7:c.3828+2T>A
(FANCA)
|
ENSP00000373952.3:n.3828+2T>A
|
|
|
ENST00000564475.5:c.158+2T>A
(FANCA)
|
|
|
|
ENST00000564870.1:c.30-703T>A
(FANCA)
|
|
|
|
ENST00000564969.5:n.113+2T>A
(FANCA)
|
|
|
|
ENST00000567879.5:c.306+2T>A
(FANCA)
|
ENSP00000457006.1:n.306+2T>A
|
|
|
ENST00000568369.5:c.3828+2T>A
(FANCA)
|
ENSP00000456829.1:n.3828+2T>A
|
|
|
ENST00000568626.1:c.537+2T>A
(FANCA)
|
|
|
|
NM_000135.2:c.3828+2T>A , LRG_495t1:c.3828+2T>A
(FANCA)
|
NP_000126.2:n.3828+2T>A
|
|
|
NM_001113525.1:c.*2556A>T
(ZNF276)
|
NP_001106997.1:n.*2556A>T
|
|
|
NM_001286167.1:c.3828+2T>A
(FANCA)
|
NP_001273096.1:n.3828+2T>A
|
|
|
NM_152287.3:c.*2556A>T
(ZNF276)
|
NP_689500.2:n.*2556A>T
|
|
|
XM_005256294.3:c.3828+2T>A
(FANCA)
|
XP_005256351.1:n.3828+2T>A
|
|
|
XM_011522945.1:c.3699+2T>A
(FANCA)
|
XP_011521247.1:n.3699+2T>A
|
|
|
XM_011522946.1:c.2805+2T>A
(FANCA)
|
XP_011521248.1:n.2805+2T>A
|
|
|
XM_011522947.1:c.2805+2T>A
(FANCA)
|
XP_011521249.1:n.2805+2T>A
|
|
|
XR_933244.1:n.3871+2T>A
(FANCA)
|
|
|
|
XR_933245.1:n.3732+2T>A
(FANCA)
|
|
|
|
XR_933246.1:n.3698+2T>A
(FANCA)
|
|
|
|
NM_000135.3:c.3828+2T>A
(FANCA)
|
NP_000126.2:n.3828+2T>A
|
|
|
NM_001286167.2:c.3828+2T>A
(FANCA)
|
NP_001273096.1:n.3828+2T>A
|
|
|
XM_005256294.4:c.3828+2T>A
(FANCA)
|
XP_005256351.1:n.3828+2T>A
|
|
|
XM_011522945.2:c.3699+2T>A
(FANCA)
|
XP_011521247.1:n.3699+2T>A
|
|
|
XM_011522946.3:c.2805+2T>A
(FANCA)
|
XP_011521248.1:n.2805+2T>A
|
|
|
XM_011522947.2:c.2805+2T>A
(FANCA)
|
XP_011521249.1:n.2805+2T>A
|
|
|
XM_017023044.2:c.3699+2T>A
(FANCA)
|
XP_016878533.1:n.3699+2T>A
|
|
|
XM_024450189.1:c.2805+2T>A
(FANCA)
|
XP_024305957.1:n.2805+2T>A
|
|
|
XR_001751866.1:n.3698+2T>A
(FANCA)
|
|
|
|
XR_933244.2:n.3871+2T>A
(FANCA)
|
|
|
|
XR_933245.2:n.3732+2T>A
(FANCA)
|
|
|
|
NM_000135.4:c.3828+2T>A
(FANCA)
MANE Select
|
NP_000126.2:n.3828+2T>A
|
|
|
NM_001113525.2:c.*2556A>T
(ZNF276)
MANE Select
|
NP_001106997.1:n.*2556A>T
|
|
|
NM_001286167.3:c.3828+2T>A
(FANCA)
|
NP_001273096.1:n.3828+2T>A
|
|
|
NM_152287.4:c.*2556A>T
(ZNF276)
|
NP_689500.2:n.*2556A>T
|
|
|
NR_110122.2:n.4556A>T
(ZNF276)
|
|
|
|
NR_110126.2:n.4439A>T
(ZNF276)
|
|
|
|
NR_110129.2:n.4473A>T
(ZNF276)
|
|
|
|
NR_110128.2:n.4379A>T
(ZNF276)
|
|
|
