|
ENST00000378043.9:c.1033C>T
(BEST1)
MANE Select
|
ENSP00000367282.4:p.Pro345Ser
|
|
|
ENST00000378043.8:c.1033C>T
(BEST1)
|
ENSP00000367282.4:p.Pro345Ser
|
|
|
ENST00000449131.6:c.853C>T
(BEST1)
|
ENSP00000399709.2:p.Pro285Ser
|
|
|
ENST00000524877.5:n.2664C>T
(BEST1)
|
|
|
|
ENST00000524926.5:c.1236C>T
(BEST1)
|
ENSP00000432681.1:p.Ser412=
|
|
|
ENST00000526988.1:c.918C>T
(BEST1)
|
ENSP00000433195.1:p.Ser306=
|
|
|
ENST00000529191.5:c.115-49G>A
(FTH1)
|
ENSP00000431659.1:n.115-49G>A
|
|
|
ENST00000529631.5:c.115-72G>A
(FTH1)
|
ENSP00000431575.1:n.115-72G>A
|
|
|
ENST00000530019.5:c.262-72G>A
(FTH1)
|
ENSP00000433470.1:n.262-72G>A
|
|
|
ENST00000534553.5:c.164-2279C>T
(BEST1)
|
ENSP00000431189.1:n.164-2279C>T
|
|
|
NM_001139443.1:c.853C>T
(BEST1)
|
NP_001132915.1:p.Pro285Ser
|
|
|
NM_001300786.1:c.772C>T
(BEST1)
|
NP_001287715.1:p.Pro258Ser
|
|
|
NM_001300787.1:c.853C>T
(BEST1)
|
NP_001287716.1:p.Pro285Ser
|
|
|
NM_004183.3:c.1033C>T
(BEST1)
|
NP_004174.1:p.Pro345Ser
|
|
|
XM_005274210.2:c.1033C>T
(BEST1)
|
XP_005274267.1:p.Pro345Ser
|
|
|
XM_005274215.2:c.715C>T
(BEST1)
|
XP_005274272.1:p.Pro239Ser
|
|
|
XM_005274216.2:c.1056C>T
(BEST1)
|
XP_005274273.1:p.Ser352=
|
|
|
XM_005274218.3:c.918C>T
(BEST1)
|
XP_005274275.1:p.Ser306=
|
|
|
XM_005274219.2:c.867+1678C>T
(BEST1)
|
XP_005274276.1:n.867+1678C>T
|
|
|
XM_005274221.2:c.715-2279C>T
(BEST1)
|
XP_005274278.1:n.715-2279C>T
|
|
|
XM_011545229.1:c.1033C>T
(BEST1)
|
XP_011543531.1:p.Pro345Ser
|
|
|
XM_011545230.1:c.940C>T
(BEST1)
|
XP_011543532.1:p.Pro314Ser
|
|
|
XM_011545231.1:c.715C>T
(BEST1)
|
XP_011543533.1:p.Pro239Ser
|
|
|
XM_011545232.1:c.1236C>T
(BEST1)
|
XP_011543534.1:p.Ser412=
|
|
|
XM_011545233.1:c.190C>T
(BEST1)
|
XP_011543535.1:p.Pro64Ser
|
|
|
NM_001363591.1:c.715C>T
(BEST1)
|
NP_001350520.1:p.Pro239Ser
|
|
|
NM_001363592.1:c.1236C>T
(BEST1)
|
NP_001350521.1:p.Ser412=
|
|
|
NM_001363593.1:c.61C>T
(BEST1)
|
NP_001350522.1:p.Pro21Ser
|
|
|
NR_134580.1:n.1816C>T
(BEST1)
|
|
|
|
XM_005274210.4:c.1033C>T
(BEST1)
|
XP_005274267.1:p.Pro345Ser
|
|
|
XM_005274215.4:c.715C>T
(BEST1)
|
XP_005274272.1:p.Pro239Ser
|
|
|
XM_005274216.4:c.1056C>T
(BEST1)
|
XP_005274273.1:p.Ser352=
|
|
|
XM_005274219.4:c.867+1678C>T
(BEST1)
|
XP_005274276.1:n.867+1678C>T
|
|
|
XM_005274221.4:c.715-2279C>T
(BEST1)
|
XP_005274278.1:n.715-2279C>T
|
|
|
XM_011545229.3:c.1033C>T
(BEST1)
|
XP_011543531.1:p.Pro345Ser
|
|
|
XM_011545230.3:c.940C>T
(BEST1)
|
XP_011543532.1:p.Pro314Ser
|
|
|
XM_011545233.3:c.190C>T
(BEST1)
|
XP_011543535.1:p.Pro64Ser
|
|
|
XM_017018230.2:c.918C>T
(BEST1)
|
XP_016873719.1:p.Ser306=
|
|
|
XR_001747952.2:n.1734C>T
(BEST1)
|
|
|
|
XR_001747953.2:n.1557+1678C>T
(BEST1)
|
|
|
|
XR_001747954.2:n.1405-2279C>T
(BEST1)
|
|
|
|
NM_004183.4:c.1033C>T
(BEST1)
MANE Select
|
NP_004174.1:p.Pro345Ser
|
|
|
NM_001139443.2:c.853C>T
(BEST1)
|
NP_001132915.1:p.Pro285Ser
|
|
|
NM_001300786.2:c.772C>T
(BEST1)
|
NP_001287715.1:p.Pro258Ser
|
|
|
NM_001300787.2:c.853C>T
(BEST1)
|
NP_001287716.1:p.Pro285Ser
|
|
|
NM_001363591.2:c.715C>T
(BEST1)
|
NP_001350520.1:p.Pro239Ser
|
|
|
NM_001363593.2:c.61C>T
(BEST1)
|
NP_001350522.1:p.Pro21Ser
|
|
|
NR_134580.2:n.1349C>T
(BEST1)
|
|
|
