ENST00000681993.1:n.642C>A
|
|
|
ENST00000682295.1:c.303+173C>A
|
ENSP00000507499.1:n.303+173C>A
|
|
ENST00000682303.1:c.*2876C>A
|
ENSP00000508325.1:n.*2876C>A
|
|
ENST00000682308.1:c.3090C>A
|
ENSP00000507056.1:p.Thr1030=
|
|
ENST00000682480.1:c.3108C>A
|
ENSP00000508344.1:p.Thr1036=
|
|
ENST00000682546.1:c.3087C>A
|
ENSP00000508188.1:p.Thr1029=
|
|
ENST00000682585.1:c.3090C>A
|
ENSP00000506885.1:p.Thr1030=
|
|
ENST00000682595.1:n.3674C>A
|
|
|
ENST00000682607.1:c.1508C>A
|
|
|
ENST00000682779.1:c.3081C>A
|
ENSP00000507947.1:p.Thr1027=
|
|
ENST00000682845.1:n.2192C>A
|
|
|
ENST00000682885.1:c.3045C>A
|
ENSP00000508036.1:p.Thr1015=
|
|
ENST00000682933.1:n.3164C>A
|
|
|
ENST00000683072.1:n.3674C>A
|
|
|
ENST00000683080.1:n.709C>A
|
|
|
ENST00000683125.1:c.3198C>A
|
ENSP00000507939.1:p.Thr1066=
|
|
ENST00000683213.1:c.3093C>A
|
ENSP00000507751.1:p.Thr1031=
|
|
ENST00000683220.1:c.3120C>A
|
ENSP00000507151.1:p.Thr1040=
|
|
ENST00000683329.1:n.3893C>A
|
|
|
ENST00000683346.1:c.*2965C>A
|
ENSP00000507458.1:n.*2965C>A
|
|
ENST00000683409.1:n.1697C>A
|
|
|
ENST00000683459.1:n.3677C>A
|
|
|
ENST00000683590.1:c.2897-5525C>A
|
ENSP00000506820.1:n.2897-5525C>A
|
|
ENST00000683623.1:c.2997C>A
|
ENSP00000507702.1:p.Thr999=
|
|
ENST00000683645.1:n.3641C>A
|
|
|
ENST00000683796.1:c.*2962C>A
|
ENSP00000508221.1:n.*2962C>A
|
|
ENST00000683802.1:n.6015C>A
|
|
|
ENST00000683833.1:c.3081C>A
|
ENSP00000506852.1:p.Thr1027=
|
|
ENST00000683994.1:c.3090C>A
|
ENSP00000507181.1:p.Thr1030=
|
|
ENST00000684290.1:c.*626C>A
|
ENSP00000507243.1:n.*626C>A
|
|
ENST00000684306.1:c.*3003C>A
|
ENSP00000508384.1:n.*3003C>A
|
|
ENST00000684341.1:n.3110C>A
|
|
|
ENST00000684383.1:c.*2728C>A
|
ENSP00000506863.1:n.*2728C>A
|
|
ENST00000684619.1:c.*2962C>A
|
ENSP00000508088.1:n.*2962C>A
|
|
ENST00000684705.1:n.211C>A
|
|
|
ENST00000684743.1:n.4121C>A
|
|
|
ENST00000260665.12:c.3090C>A
MANE Select
|
ENSP00000260665.7:p.Thr1030=
|
|
ENST00000260665.11:c.3090C>A
|
ENSP00000260665.7:p.Thr1030=
|
|
NM_133259.3:c.3090C>A
|
NP_573566.2:p.Thr1030=
|
|
XM_006711915.2:c.3012C>A
|
XP_006711978.1:p.Thr1004=
|
|
XM_006711916.2:c.3090C>A
|
XP_006711979.1:p.Thr1030=
|
|
XM_011532473.1:c.3090C>A
|
XP_011530775.1:p.Thr1030=
|
|
XM_011532474.1:c.3090C>A
|
XP_011530776.1:p.Thr1030=
|
|
XM_006711916.3:c.3090C>A
|
XP_006711979.1:p.Thr1030=
|
|
XM_017003117.1:c.3012C>A
|
XP_016858606.1:p.Thr1004=
|
|
XR_002958896.1:n.3132C>A
|
|
|
NM_133259.4:c.3090C>A
MANE Select
|
NP_573566.2:p.Thr1030=
|
|