|
ENST00000681993.1:n.508G=
|
|
|
|
ENST00000682295.1:c.220G=
|
ENSP00000507499.1:p.Val74=
|
|
|
ENST00000682303.1:c.*2742G=
|
ENSP00000508325.1:n.*2742G=
|
|
|
ENST00000682308.1:c.2956G=
|
ENSP00000507056.1:p.Val986=
|
|
|
ENST00000682480.1:c.2956G=
|
ENSP00000508344.1:p.Val986=
|
|
|
ENST00000682546.1:c.2953G=
|
ENSP00000508188.1:p.Val985=
|
|
|
ENST00000682585.1:c.2956G=
|
ENSP00000506885.1:p.Val986=
|
|
|
ENST00000682595.1:n.3540G=
|
|
|
|
ENST00000682607.1:c.1374G=
|
|
|
|
ENST00000682779.1:c.2947G=
|
ENSP00000507947.1:p.Val983=
|
|
|
ENST00000682845.1:n.2058G=
|
|
|
|
ENST00000682885.1:c.2911G=
|
ENSP00000508036.1:p.Val971=
|
|
|
ENST00000682933.1:n.3030G=
|
|
|
|
ENST00000683072.1:n.3540G=
|
|
|
|
ENST00000683080.1:n.575G=
|
|
|
|
ENST00000683125.1:c.3064G=
|
ENSP00000507939.1:p.Val1022=
|
|
|
ENST00000683213.1:c.2959G=
|
ENSP00000507751.1:p.Val987=
|
|
|
ENST00000683220.1:c.2986G=
|
ENSP00000507151.1:p.Val996=
|
|
|
ENST00000683236.1:c.286G=
|
ENSP00000506891.1:n.286G=
|
|
|
ENST00000683329.1:n.3759G=
|
|
|
|
ENST00000683346.1:c.*2831G=
|
ENSP00000507458.1:n.*2831G=
|
|
|
ENST00000683409.1:n.1563G=
|
|
|
|
ENST00000683459.1:n.3543G=
|
|
|
|
ENST00000683590.1:c.2897-5781G=
|
ENSP00000506820.1:n.2897-5781G=
|
|
|
ENST00000683623.1:c.2863G=
|
ENSP00000507702.1:p.Val955=
|
|
|
ENST00000683645.1:n.3507G=
|
|
|
|
ENST00000683796.1:c.*2828G=
|
ENSP00000508221.1:n.*2828G=
|
|
|
ENST00000683802.1:n.5881G=
|
|
|
|
ENST00000683833.1:c.2947G=
|
ENSP00000506852.1:p.Val983=
|
|
|
ENST00000683994.1:c.2956G=
|
ENSP00000507181.1:p.Val986=
|
|
|
ENST00000684290.1:c.*492G=
|
ENSP00000507243.1:n.*492G=
|
|
|
ENST00000684306.1:c.*2869G=
|
ENSP00000508384.1:n.*2869G=
|
|
|
ENST00000684341.1:n.2976G=
|
|
|
|
ENST00000684383.1:c.*2594G=
|
ENSP00000506863.1:n.*2594G=
|
|
|
ENST00000684619.1:c.*2828G=
|
ENSP00000508088.1:n.*2828G=
|
|
|
ENST00000684705.1:n.77G=
|
|
|
|
ENST00000684743.1:n.3987G=
|
|
|
|
ENST00000260665.12:c.2956G=
MANE Select
|
ENSP00000260665.7:p.Val986=
|
|
|
ENST00000260665.11:c.2956G=
|
ENSP00000260665.7:p.Val986=
|
|
|
NM_133259.3:c.2956G=
|
NP_573566.2:p.Val986=
|
|
|
XM_006711915.2:c.2878G=
|
XP_006711978.1:p.Val960=
|
|
|
XM_006711916.2:c.2956G=
|
XP_006711979.1:p.Val986=
|
|
|
XM_011532473.1:c.2956G=
|
XP_011530775.1:p.Val986=
|
|
|
XM_011532474.1:c.2956G=
|
XP_011530776.1:p.Val986=
|
|
|
XM_006711916.3:c.2956G=
|
XP_006711979.1:p.Val986=
|
|
|
XM_017003117.1:c.2878G=
|
XP_016858606.1:p.Val960=
|
|
|
XR_002958896.1:n.2998G=
|
|
|
|
NM_133259.4:c.2956G=
MANE Select
|
NP_573566.2:p.Val986=
|
|
