|
ENST00000378043.9:c.983A>T
(BEST1)
MANE Select
|
ENSP00000367282.4:p.Asp328Val
|
|
|
ENST00000378043.8:c.983A>T
(BEST1)
|
ENSP00000367282.4:p.Asp328Val
|
|
|
ENST00000449131.6:c.803A>T
(BEST1)
|
ENSP00000399709.2:p.Asp268Val
|
|
|
ENST00000524877.5:n.2614A>T
(BEST1)
|
|
|
|
ENST00000524926.5:c.1186A>T
(BEST1)
|
ENSP00000432681.1:p.Thr396Ser
|
|
|
ENST00000526988.1:c.868A>T
(BEST1)
|
ENSP00000433195.1:p.Thr290Ser
|
|
|
ENST00000529191.5:c.116T>A
(FTH1)
|
ENSP00000431659.1:p.Val39Asp
|
|
|
ENST00000529631.5:c.115-22T>A
(FTH1)
|
ENSP00000431575.1:n.115-22T>A
|
|
|
ENST00000530019.5:c.262-22T>A
(FTH1)
|
ENSP00000433470.1:n.262-22T>A
|
|
|
ENST00000534553.5:c.164-2329A>T
(BEST1)
|
ENSP00000431189.1:n.164-2329A>T
|
|
|
NM_001139443.1:c.803A>T
(BEST1)
|
NP_001132915.1:p.Asp268Val
|
|
|
NM_001300786.1:c.722A>T
(BEST1)
|
NP_001287715.1:p.Asp241Val
|
|
|
NM_001300787.1:c.803A>T
(BEST1)
|
NP_001287716.1:p.Asp268Val
|
|
|
NM_004183.3:c.983A>T
(BEST1)
|
NP_004174.1:p.Asp328Val
|
|
|
XM_005274210.2:c.983A>T
(BEST1)
|
XP_005274267.1:p.Asp328Val
|
|
|
XM_005274215.2:c.665A>T
(BEST1)
|
XP_005274272.1:p.Asp222Val
|
|
|
XM_005274216.2:c.1006A>T
(BEST1)
|
XP_005274273.1:p.Thr336Ser
|
|
|
XM_005274218.3:c.868A>T
(BEST1)
|
XP_005274275.1:p.Thr290Ser
|
|
|
XM_005274219.2:c.867+1628A>T
(BEST1)
|
XP_005274276.1:n.867+1628A>T
|
|
|
XM_005274221.2:c.715-2329A>T
(BEST1)
|
XP_005274278.1:n.715-2329A>T
|
|
|
XM_011545229.1:c.983A>T
(BEST1)
|
XP_011543531.1:p.Asp328Val
|
|
|
XM_011545230.1:c.890A>T
(BEST1)
|
XP_011543532.1:p.Asp297Val
|
|
|
XM_011545231.1:c.665A>T
(BEST1)
|
XP_011543533.1:p.Asp222Val
|
|
|
XM_011545232.1:c.1186A>T
(BEST1)
|
XP_011543534.1:p.Thr396Ser
|
|
|
XM_011545233.1:c.140A>T
(BEST1)
|
XP_011543535.1:p.Asp47Val
|
|
|
NM_001363591.1:c.665A>T
(BEST1)
|
NP_001350520.1:p.Asp222Val
|
|
|
NM_001363592.1:c.1186A>T
(BEST1)
|
NP_001350521.1:p.Thr396Ser
|
|
|
NM_001363593.1:c.11A>T
(BEST1)
|
NP_001350522.1:p.Asp4Val
|
|
|
NR_134580.1:n.1766A>T
(BEST1)
|
|
|
|
XM_005274210.4:c.983A>T
(BEST1)
|
XP_005274267.1:p.Asp328Val
|
|
|
XM_005274215.4:c.665A>T
(BEST1)
|
XP_005274272.1:p.Asp222Val
|
|
|
XM_005274216.4:c.1006A>T
(BEST1)
|
XP_005274273.1:p.Thr336Ser
|
|
|
XM_005274219.4:c.867+1628A>T
(BEST1)
|
XP_005274276.1:n.867+1628A>T
|
|
|
XM_005274221.4:c.715-2329A>T
(BEST1)
|
XP_005274278.1:n.715-2329A>T
|
|
|
XM_011545229.3:c.983A>T
(BEST1)
|
XP_011543531.1:p.Asp328Val
|
|
|
XM_011545230.3:c.890A>T
(BEST1)
|
XP_011543532.1:p.Asp297Val
|
|
|
XM_011545233.3:c.140A>T
(BEST1)
|
XP_011543535.1:p.Asp47Val
|
|
|
XM_017018230.2:c.868A>T
(BEST1)
|
XP_016873719.1:p.Thr290Ser
|
|
|
XR_001747952.2:n.1684A>T
(BEST1)
|
|
|
|
XR_001747953.2:n.1557+1628A>T
(BEST1)
|
|
|
|
XR_001747954.2:n.1405-2329A>T
(BEST1)
|
|
|
|
XR_001748245.1:n.2T>A
|
|
|
|
XR_002957249.1:n.2T>A
|
|
|
|
NM_004183.4:c.983A>T
(BEST1)
MANE Select
|
NP_004174.1:p.Asp328Val
|
|
|
NM_001139443.2:c.803A>T
(BEST1)
|
NP_001132915.1:p.Asp268Val
|
|
|
NM_001300786.2:c.722A>T
(BEST1)
|
NP_001287715.1:p.Asp241Val
|
|
|
NM_001300787.2:c.803A>T
(BEST1)
|
NP_001287716.1:p.Asp268Val
|
|
|
NM_001363591.2:c.665A>T
(BEST1)
|
NP_001350520.1:p.Asp222Val
|
|
|
NM_001363593.2:c.11A>T
(BEST1)
|
NP_001350522.1:p.Asp4Val
|
|
|
NR_134580.2:n.1299A>T
(BEST1)
|
|
|
