|
ENST00000710812.1:n.410+26377G>A
(AOPEP)
|
|
|
|
ENST00000696260.1:n.2257C>T
(FANCC)
|
|
|
|
ENST00000289081.8:c.1442C>T
(FANCC)
MANE Select
|
ENSP00000289081.3:p.Ala481Val
|
|
|
ENST00000375305.6:c.1442C>T
(FANCC)
|
ENSP00000364454.1:p.Ala481Val
|
|
|
ENST00000649334.1:c.1587C>T
(FANCC)
|
ENSP00000497735.1:n.1587C>T
|
|
|
ENST00000289081.7:c.1442C>T
(FANCC)
|
ENSP00000289081.3:p.Ala481Val
|
|
|
ENST00000375305.5:c.1442C>T
(FANCC)
|
ENSP00000364454.1:p.Ala481Val
|
|
|
ENST00000464627.5:n.769C>T
(FANCC)
|
|
|
|
NM_000136.2:c.1442C>T , LRG_497t1:c.1442C>T
(FANCC)
|
NP_000127.2:p.Ala481Val
|
|
|
NM_001243743.1:c.1442C>T
(FANCC)
|
NP_001230672.1:p.Ala481Val
|
|
|
XM_005251802.2:c.761C>T
(FANCC)
|
XP_005251859.1:p.Ala254Val
|
|
|
XM_006717001.1:c.1277C>T
(FANCC)
|
XP_006717064.1:p.Ala426Val
|
|
|
XM_011518365.1:c.1442C>T
(FANCC)
|
XP_011516667.1:p.Ala481Val
|
|
|
XM_011518367.1:c.986C>T
(FANCC)
|
XP_011516669.1:p.Ala329Val
|
|
|
XM_011519121.1:c.2319+26377G>A
(AOPEP)
|
XP_011517423.1:n.2319+26377G>A
|
|
|
XM_005251802.3:c.761C>T
(FANCC)
|
XP_005251859.1:p.Ala254Val
|
|
|
XM_006717001.3:c.1277C>T
(FANCC)
|
XP_006717064.1:p.Ala426Val
|
|
|
XM_011518365.3:c.1442C>T
(FANCC)
|
XP_011516667.1:p.Ala481Val
|
|
|
XM_011518367.2:c.986C>T
(FANCC)
|
XP_011516669.1:p.Ala329Val
|
|
|
XM_011519121.3:c.2319+26377G>A
(AOPEP)
|
XP_011517423.1:n.2319+26377G>A
|
|
|
XM_017014452.2:c.986C>T
(FANCC)
|
XP_016869941.1:p.Ala329Val
|
|
|
XM_017014453.1:c.986C>T
(FANCC)
|
XP_016869942.1:p.Ala329Val
|
|
|
XM_017014454.1:c.821C>T
(FANCC)
|
XP_016869943.1:p.Ala274Val
|
|
|
XM_024447451.1:c.1442C>T
(FANCC)
|
XP_024303219.1:p.Ala481Val
|
|
|
XR_001746847.1:n.575G>A
|
|
|
|
NM_000136.3:c.1442C>T
(FANCC)
MANE Select
|
NP_000127.2:p.Ala481Val
|
|
|
NM_001243743.2:c.1442C>T
(FANCC)
|
NP_001230672.1:p.Ala481Val
|
|
