ENST00000710812.1:n.411-11736A>C
(AOPEP)
|
|
|
ENST00000696261.1:n.1105T>G
(FANCC)
|
|
|
ENST00000289081.8:c.714T>G
(FANCC)
MANE Select
|
ENSP00000289081.3:p.Ala238=
|
|
ENST00000375305.6:c.714T>G
(FANCC)
|
ENSP00000364454.1:p.Ala238=
|
|
ENST00000490972.7:c.714T>G
(FANCC)
|
ENSP00000479931.1:p.Ala238=
|
|
ENST00000649334.1:c.859T>G
(FANCC)
|
ENSP00000497735.1:n.859T>G
|
|
ENST00000649701.1:n.429T>G
(FANCC)
|
|
|
ENST00000289081.7:c.714T>G
(FANCC)
|
ENSP00000289081.3:p.Ala238=
|
|
ENST00000375305.5:c.714T>G
(FANCC)
|
ENSP00000364454.1:p.Ala238=
|
|
ENST00000477942.5:n.69T>G
(FANCC)
|
|
|
ENST00000490972.6:c.714T>G
(FANCC)
|
ENSP00000479931.1:p.Ala238=
|
|
NM_000136.2:c.714T>G , LRG_497t1:c.714T>G
(FANCC)
|
NP_000127.2:p.Ala238=
|
|
NM_001243743.1:c.714T>G
(FANCC)
|
NP_001230672.1:p.Ala238=
|
|
NM_001243744.1:c.714T>G
(FANCC)
|
NP_001230673.1:p.Ala238=
|
|
XM_005251802.2:c.33T>G
(FANCC)
|
XP_005251859.1:p.Ala11=
|
|
XM_006717001.1:c.549T>G
(FANCC)
|
XP_006717064.1:p.Ala183=
|
|
XM_006717002.2:c.714T>G
(FANCC)
|
XP_006717065.1:p.Ala238=
|
|
XM_006717004.2:c.714T>G
(FANCC)
|
XP_006717067.1:p.Ala238=
|
|
XM_011518365.1:c.714T>G
(FANCC)
|
XP_011516667.1:p.Ala238=
|
|
XM_011518366.1:c.714T>G
(FANCC)
|
XP_011516668.1:p.Ala238=
|
|
XM_011518367.1:c.258T>G
(FANCC)
|
XP_011516669.1:p.Ala86=
|
|
XM_011519121.1:c.2320-11736A>C
(AOPEP)
|
XP_011517423.1:n.2320-11736A>C
|
|
XM_005251802.3:c.33T>G
(FANCC)
|
XP_005251859.1:p.Ala11=
|
|
XM_006717001.3:c.549T>G
(FANCC)
|
XP_006717064.1:p.Ala183=
|
|
XM_006717002.4:c.714T>G
(FANCC)
|
XP_006717065.1:p.Ala238=
|
|
XM_006717004.4:c.714T>G
(FANCC)
|
XP_006717067.1:p.Ala238=
|
|
XM_011518365.3:c.714T>G
(FANCC)
|
XP_011516667.1:p.Ala238=
|
|
XM_011518366.3:c.714T>G
(FANCC)
|
XP_011516668.1:p.Ala238=
|
|
XM_011518367.2:c.258T>G
(FANCC)
|
XP_011516669.1:p.Ala86=
|
|
XM_011519121.3:c.2320-11736A>C
(AOPEP)
|
XP_011517423.1:n.2320-11736A>C
|
|
XM_017014452.2:c.258T>G
(FANCC)
|
XP_016869941.1:p.Ala86=
|
|
XM_017014453.1:c.258T>G
(FANCC)
|
XP_016869942.1:p.Ala86=
|
|
XM_017014454.1:c.93T>G
(FANCC)
|
XP_016869943.1:p.Ala31=
|
|
XM_024447451.1:c.714T>G
(FANCC)
|
XP_024303219.1:p.Ala238=
|
|
NM_000136.3:c.714T>G
(FANCC)
MANE Select
|
NP_000127.2:p.Ala238=
|
|
NM_001243743.2:c.714T>G
(FANCC)
|
NP_001230672.1:p.Ala238=
|
|
NM_001243744.2:c.714T>G
(FANCC)
|
NP_001230673.1:p.Ala238=
|
|