|
ENST00000419884.6:c.569A>G
|
|
|
|
ENST00000681993.1:n.1491A>G
|
|
|
|
ENST00000682154.1:n.1373A>G
|
|
|
|
ENST00000682303.1:c.*3650A>G
|
ENSP00000508325.1:n.*3650A>G
|
|
|
ENST00000682308.1:c.3864A>G
|
ENSP00000507056.1:p.Glu1288=
|
|
|
ENST00000682434.1:n.3494A>G
|
|
|
|
ENST00000682480.1:c.3957A>G
|
ENSP00000508344.1:p.Glu1319=
|
|
|
ENST00000682546.1:c.3936A>G
|
ENSP00000508188.1:p.Glu1312=
|
|
|
ENST00000682585.1:c.*67A>G
|
ENSP00000506885.1:n.*67A>G
|
|
|
ENST00000682607.1:c.2682A>G
|
|
|
|
ENST00000682612.1:c.752+2043A>G
|
|
|
|
ENST00000682696.1:c.39A>G
|
ENSP00000508411.1:p.Glu13=
|
|
|
ENST00000682779.1:c.3930A>G
|
ENSP00000507947.1:p.Glu1310=
|
|
|
ENST00000682885.1:c.3894A>G
|
ENSP00000508036.1:p.Glu1298=
|
|
|
ENST00000682933.1:n.4139A>G
|
|
|
|
ENST00000683002.1:c.791A>G
|
|
|
|
ENST00000683072.1:n.4523A>G
|
|
|
|
ENST00000683080.1:n.1558A>G
|
|
|
|
ENST00000683096.1:n.2380A>G
|
|
|
|
ENST00000683125.1:c.4047A>G
|
ENSP00000507939.1:p.Glu1349=
|
|
|
ENST00000683213.1:c.3942A>G
|
ENSP00000507751.1:p.Glu1314=
|
|
|
ENST00000683220.1:c.3969A>G
|
ENSP00000507151.1:p.Glu1323=
|
|
|
ENST00000683329.1:n.4742A>G
|
|
|
|
ENST00000683346.1:c.*3814A>G
|
ENSP00000507458.1:n.*3814A>G
|
|
|
ENST00000683409.1:n.2471A>G
|
|
|
|
ENST00000683459.1:n.4526A>G
|
|
|
|
ENST00000683590.1:c.3612A>G
|
ENSP00000506820.1:p.Glu1204=
|
|
|
ENST00000683623.1:c.3846A>G
|
ENSP00000507702.1:p.Glu1282=
|
|
|
ENST00000683796.1:c.*3736A>G
|
ENSP00000508221.1:n.*3736A>G
|
|
|
ENST00000683833.1:c.3855A>G
|
ENSP00000506852.1:p.Glu1285=
|
|
|
ENST00000683994.1:c.*52A>G
|
ENSP00000507181.1:n.*52A>G
|
|
|
ENST00000684290.1:c.*1400A>G
|
ENSP00000507243.1:n.*1400A>G
|
|
|
ENST00000684306.1:c.*3852A>G
|
ENSP00000508384.1:n.*3852A>G
|
|
|
ENST00000684383.1:c.*3577A>G
|
ENSP00000506863.1:n.*3577A>G
|
|
|
ENST00000684418.1:n.5120A>G
|
|
|
|
ENST00000684433.1:n.323A>G
|
|
|
|
ENST00000684454.1:n.7803A>G
|
|
|
|
ENST00000684619.1:c.*3811A>G
|
ENSP00000508088.1:n.*3811A>G
|
|
|
ENST00000684743.1:n.6684A>G
|
|
|
|
ENST00000260665.12:c.3939A>G
MANE Select
|
ENSP00000260665.7:p.Glu1313=
|
|
|
ENST00000260665.11:c.3939A>G
|
ENSP00000260665.7:p.Glu1313=
|
|
|
ENST00000419884.5:c.180A>G
|
ENSP00000414207.1:p.Glu60=
|
|
|
ENST00000463456.5:n.2982A>G
|
|
|
|
NM_133259.3:c.3939A>G
|
NP_573566.2:p.Glu1313=
|
|
|
XM_006711915.2:c.3861A>G
|
XP_006711978.1:p.Glu1287=
|
|
|
XM_011532473.1:c.3864A>G
|
XP_011530775.1:p.Glu1288=
|
|
|
XM_011532474.1:c.3939A>G
|
XP_011530776.1:p.Glu1313=
|
|
|
XM_017003117.1:c.3786A>G
|
XP_016858606.1:p.Glu1262=
|
|
|
XR_002958896.1:n.3981A>G
|
|
|
|
NM_133259.4:c.3939A>G
MANE Select
|
NP_573566.2:p.Glu1313=
|
|
