|
ENST00000433342.6:c.3443A>T
(C1orf167)
|
ENSP00000414909.3:p.Glu1148Val
|
|
|
ENST00000688073.1:c.3944A>T
(C1orf167)
MANE Select
|
ENSP00000510540.1:p.Glu1315Val
|
|
|
ENST00000376585.6:c.*2436T>A
(MTHFR)
|
ENSP00000365770.1:n.*2436T>A
|
|
|
ENST00000376590.9:c.*2436T>A
(MTHFR)
MANE Select
|
ENSP00000365775.3:n.*2436T>A
|
|
|
ENST00000376592.6:c.*2436T>A
(MTHFR)
|
ENSP00000365777.1:n.*2436T>A
|
|
|
ENST00000312793.9:c.2079A>T
(C1orf167)
|
|
|
|
ENST00000376583.7:c.4530T>A
(MTHFR)
|
ENSP00000365767.3:n.4530T>A
|
|
|
ENST00000376590.7:c.*2436T>A
(MTHFR)
|
ENSP00000365775.3:n.*2436T>A
|
|
|
ENST00000376592.5:c.*2436T>A
(MTHFR)
|
ENSP00000365777.1:n.*2436T>A
|
|
|
ENST00000433342.5:c.4001A>T
(C1orf167)
|
ENSP00000414909.2:p.Glu1334Val
|
|
|
ENST00000444493.5:c.1443A>T
(C1orf167)
|
|
|
|
ENST00000449278.1:c.1179A>T
(C1orf167)
|
|
|
|
ENST00000482358.1:n.238A>T
(C1orf167)
|
|
|
|
NM_001010881.1:c.3944A>T
(C1orf167)
|
NP_001010881.1:p.Glu1315Val
|
|
|
NM_005957.4:c.*2436T>A , LRG_726t1:c.*2436T>A
(MTHFR)
|
NP_005948.3:n.*2436T>A
|
|
|
XM_006711078.2:c.3944A>T
(C1orf167)
|
XP_006711141.1:p.Glu1315Val
|
|
|
XM_011541267.1:c.4079A>T
(C1orf167)
|
XP_011539569.1:p.Glu1360Val
|
|
|
XM_011541268.1:c.4079A>T
(C1orf167)
|
XP_011539570.1:p.Glu1360Val
|
|
|
XM_011541269.1:c.4079A>T
(C1orf167)
|
XP_011539571.1:p.Glu1360Val
|
|
|
XM_011541270.1:c.4079A>T
(C1orf167)
|
XP_011539572.1:p.Glu1360Val
|
|
|
XM_011541271.1:c.4025A>T
(C1orf167)
|
XP_011539573.1:p.Glu1342Val
|
|
|
XM_011541272.1:c.4079A>T
(C1orf167)
|
XP_011539574.1:p.Glu1360Val
|
|
|
XM_011541273.1:c.3944A>T
(C1orf167)
|
XP_011539575.1:p.Glu1315Val
|
|
|
XM_011541274.1:c.3944A>T
(C1orf167)
|
XP_011539576.1:p.Glu1315Val
|
|
|
XM_011541275.1:c.3944A>T
(C1orf167)
|
XP_011539577.1:p.Glu1315Val
|
|
|
XM_011541276.1:c.3985A>T
(C1orf167)
|
XP_011539578.1:p.Arg1329Trp
|
|
|
XM_011541277.1:c.3985A>T
(C1orf167)
|
XP_011539579.1:p.Arg1329Trp
|
|
|
XM_011541278.1:c.4079A>T
(C1orf167)
|
XP_011539580.1:p.Glu1360Val
|
|
|
XM_011541279.1:c.3671A>T
(C1orf167)
|
XP_011539581.1:p.Glu1224Val
|
|
|
XM_011541280.1:c.2360A>T
(C1orf167)
|
XP_011539582.1:p.Glu787Val
|
|
|
XM_011541281.1:c.2360A>T
(C1orf167)
|
XP_011539583.1:p.Glu787Val
|
|
|
NM_001330358.1:c.*2436T>A
(MTHFR)
|
NP_001317287.1:n.*2436T>A
|
|
|
XM_011541272.3:c.4079A>T
(C1orf167)
|
XP_011539574.1:p.Glu1360Val
|
|
|
XM_011541276.3:c.3985A>T
(C1orf167)
|
XP_011539578.1:p.Arg1329Trp
|
|
|
XM_011541277.3:c.3985A>T
(C1orf167)
|
XP_011539579.1:p.Arg1329Trp
|
|
|
XM_011541278.2:c.4079A>T
(C1orf167)
|
XP_011539580.1:p.Glu1360Val
|
|
|
XM_024446506.1:c.4079A>T
(C1orf167)
|
XP_024302274.1:p.Glu1360Val
|
|
|
XM_024446507.1:c.4079A>T
(C1orf167)
|
XP_024302275.1:p.Glu1360Val
|
|
|
XM_024446508.1:c.4079A>T
(C1orf167)
|
XP_024302276.1:p.Glu1360Val
|
|
|
XM_024446509.1:c.4079A>T
(C1orf167)
|
XP_024302277.1:p.Glu1360Val
|
|
|
XM_024446512.1:c.4025A>T
(C1orf167)
|
XP_024302280.1:p.Glu1342Val
|
|
|
XM_024446514.1:c.3944A>T
(C1orf167)
|
XP_024302282.1:p.Glu1315Val
|
|
|
XM_024446515.1:c.3944A>T
(C1orf167)
|
XP_024302283.1:p.Glu1315Val
|
|
|
XM_024446517.1:c.3944A>T
(C1orf167)
|
XP_024302285.1:p.Glu1315Val
|
|
|
XM_024446518.1:c.2360A>T
(C1orf167)
|
XP_024302286.1:p.Glu787Val
|
|
|
NM_001010881.2:c.3944A>T
(C1orf167)
MANE Select
|
NP_001010881.1:p.Glu1315Val
|
|
|
NM_005957.5:c.*2436T>A
(MTHFR)
MANE Select
|
NP_005948.3:n.*2436T>A
|
|
|
NM_001330358.2:c.*2436T>A
(MTHFR)
|
NP_001317287.1:n.*2436T>A
|
|
