ENST00000710812.1:n.410+30762T>A
(AOPEP)
|
|
|
ENST00000696260.1:n.2065A>T
(FANCC)
|
|
|
ENST00000289081.8:c.1250A>T
(FANCC)
MANE Select
|
ENSP00000289081.3:p.Glu417Val
|
|
ENST00000375305.6:c.1250A>T
(FANCC)
|
ENSP00000364454.1:p.Glu417Val
|
|
ENST00000490972.7:c.1250A>T
(FANCC)
|
ENSP00000479931.1:p.Glu417Val
|
|
ENST00000649334.1:c.1395A>T
(FANCC)
|
ENSP00000497735.1:n.1395A>T
|
|
ENST00000289081.7:c.1250A>T
(FANCC)
|
ENSP00000289081.3:p.Glu417Val
|
|
ENST00000375305.5:c.1250A>T
(FANCC)
|
ENSP00000364454.1:p.Glu417Val
|
|
ENST00000464627.5:n.577A>T
(FANCC)
|
|
|
ENST00000477942.5:n.605A>T
(FANCC)
|
|
|
ENST00000480712.5:n.435A>T
(FANCC)
|
|
|
ENST00000490972.6:c.1250A>T
(FANCC)
|
ENSP00000479931.1:p.Glu417Val
|
|
NM_000136.2:c.1250A>T , LRG_497t1:c.1250A>T
(FANCC)
|
NP_000127.2:p.Glu417Val
|
|
NM_001243743.1:c.1250A>T
(FANCC)
|
NP_001230672.1:p.Glu417Val
|
|
NM_001243744.1:c.1250A>T
(FANCC)
|
NP_001230673.1:p.Glu417Val
|
|
XM_005251802.2:c.569A>T
(FANCC)
|
XP_005251859.1:p.Glu190Val
|
|
XM_006717001.1:c.1085A>T
(FANCC)
|
XP_006717064.1:p.Glu362Val
|
|
XM_006717002.2:c.1250A>T
(FANCC)
|
XP_006717065.1:p.Glu417Val
|
|
XM_011518365.1:c.1250A>T
(FANCC)
|
XP_011516667.1:p.Glu417Val
|
|
XM_011518366.1:c.1250A>T
(FANCC)
|
XP_011516668.1:p.Glu417Val
|
|
XM_011518367.1:c.794A>T
(FANCC)
|
XP_011516669.1:p.Glu265Val
|
|
XM_011519121.1:c.2319+30762T>A
(AOPEP)
|
XP_011517423.1:n.2319+30762T>A
|
|
XM_005251802.3:c.569A>T
(FANCC)
|
XP_005251859.1:p.Glu190Val
|
|
XM_006717001.3:c.1085A>T
(FANCC)
|
XP_006717064.1:p.Glu362Val
|
|
XM_006717002.4:c.1250A>T
(FANCC)
|
XP_006717065.1:p.Glu417Val
|
|
XM_006717004.4:c.*145A>T
(FANCC)
|
XP_006717067.1:n.*145A>T
|
|
XM_011518365.3:c.1250A>T
(FANCC)
|
XP_011516667.1:p.Glu417Val
|
|
XM_011518366.3:c.1250A>T
(FANCC)
|
XP_011516668.1:p.Glu417Val
|
|
XM_011518367.2:c.794A>T
(FANCC)
|
XP_011516669.1:p.Glu265Val
|
|
XM_011519121.3:c.2319+30762T>A
(AOPEP)
|
XP_011517423.1:n.2319+30762T>A
|
|
XM_017014452.2:c.794A>T
(FANCC)
|
XP_016869941.1:p.Glu265Val
|
|
XM_017014453.1:c.794A>T
(FANCC)
|
XP_016869942.1:p.Glu265Val
|
|
XM_017014454.1:c.629A>T
(FANCC)
|
XP_016869943.1:p.Glu210Val
|
|
XM_024447451.1:c.1250A>T
(FANCC)
|
XP_024303219.1:p.Glu417Val
|
|
NM_000136.3:c.1250A>T
(FANCC)
MANE Select
|
NP_000127.2:p.Glu417Val
|
|
NM_001243743.2:c.1250A>T
(FANCC)
|
NP_001230672.1:p.Glu417Val
|
|
NM_001243744.2:c.1250A>T
(FANCC)
|
NP_001230673.1:p.Glu417Val
|
|