|
ENST00000419884.6:c.587A>T
|
|
|
|
ENST00000681993.1:n.1509A>T
|
|
|
|
ENST00000682154.1:n.1391A>T
|
|
|
|
ENST00000682303.1:c.*3668A>T
|
ENSP00000508325.1:n.*3668A>T
|
|
|
ENST00000682308.1:c.3882A>T
|
ENSP00000507056.1:p.Glu1294Asp
|
|
|
ENST00000682434.1:n.3512A>T
|
|
|
|
ENST00000682480.1:c.3975A>T
|
ENSP00000508344.1:p.Glu1325Asp
|
|
|
ENST00000682546.1:c.3954A>T
|
ENSP00000508188.1:p.Glu1318Asp
|
|
|
ENST00000682585.1:c.*85A>T
|
ENSP00000506885.1:n.*85A>T
|
|
|
ENST00000682607.1:c.2700A>T
|
|
|
|
ENST00000682612.1:c.752+2061A>T
|
|
|
|
ENST00000682696.1:c.57A>T
|
ENSP00000508411.1:p.Glu19Asp
|
|
|
ENST00000682779.1:c.3948A>T
|
ENSP00000507947.1:p.Glu1316Asp
|
|
|
ENST00000682885.1:c.3912A>T
|
ENSP00000508036.1:p.Glu1304Asp
|
|
|
ENST00000682933.1:n.4157A>T
|
|
|
|
ENST00000683002.1:c.809A>T
|
|
|
|
ENST00000683072.1:n.4541A>T
|
|
|
|
ENST00000683080.1:n.1576A>T
|
|
|
|
ENST00000683096.1:n.2398A>T
|
|
|
|
ENST00000683125.1:c.4065A>T
|
ENSP00000507939.1:p.Glu1355Asp
|
|
|
ENST00000683213.1:c.3960A>T
|
ENSP00000507751.1:p.Glu1320Asp
|
|
|
ENST00000683220.1:c.3987A>T
|
ENSP00000507151.1:p.Glu1329Asp
|
|
|
ENST00000683329.1:n.4760A>T
|
|
|
|
ENST00000683346.1:c.*3832A>T
|
ENSP00000507458.1:n.*3832A>T
|
|
|
ENST00000683409.1:n.2489A>T
|
|
|
|
ENST00000683459.1:n.4544A>T
|
|
|
|
ENST00000683590.1:c.3630A>T
|
ENSP00000506820.1:p.Glu1210Asp
|
|
|
ENST00000683623.1:c.3864A>T
|
ENSP00000507702.1:p.Glu1288Asp
|
|
|
ENST00000683796.1:c.*3754A>T
|
ENSP00000508221.1:n.*3754A>T
|
|
|
ENST00000683833.1:c.3873A>T
|
ENSP00000506852.1:p.Glu1291Asp
|
|
|
ENST00000683994.1:c.*70A>T
|
ENSP00000507181.1:n.*70A>T
|
|
|
ENST00000684290.1:c.*1418A>T
|
ENSP00000507243.1:n.*1418A>T
|
|
|
ENST00000684306.1:c.*3870A>T
|
ENSP00000508384.1:n.*3870A>T
|
|
|
ENST00000684383.1:c.*3595A>T
|
ENSP00000506863.1:n.*3595A>T
|
|
|
ENST00000684418.1:n.5138A>T
|
|
|
|
ENST00000684433.1:n.341A>T
|
|
|
|
ENST00000684454.1:n.7821A>T
|
|
|
|
ENST00000684619.1:c.*3829A>T
|
ENSP00000508088.1:n.*3829A>T
|
|
|
ENST00000684743.1:n.6702A>T
|
|
|
|
ENST00000260665.12:c.3957A>T
MANE Select
|
ENSP00000260665.7:p.Glu1319Asp
|
|
|
ENST00000260665.11:c.3957A>T
|
ENSP00000260665.7:p.Glu1319Asp
|
|
|
ENST00000419884.5:c.198A>T
|
ENSP00000414207.1:p.Glu66Asp
|
|
|
ENST00000463456.5:n.3000A>T
|
|
|
|
NM_133259.3:c.3957A>T
|
NP_573566.2:p.Glu1319Asp
|
|
|
XM_006711915.2:c.3879A>T
|
XP_006711978.1:p.Glu1293Asp
|
|
|
XM_011532473.1:c.3882A>T
|
XP_011530775.1:p.Glu1294Asp
|
|
|
XM_011532474.1:c.3957A>T
|
XP_011530776.1:p.Glu1319Asp
|
|
|
XM_017003117.1:c.3804A>T
|
XP_016858606.1:p.Glu1268Asp
|
|
|
XR_002958896.1:n.3999A>T
|
|
|
|
NM_133259.4:c.3957A>T
MANE Select
|
NP_573566.2:p.Glu1319Asp
|
|
