ENST00000681993.1:n.680G>A
|
|
|
ENST00000682295.1:c.303+211G>A
|
ENSP00000507499.1:n.303+211G>A
|
|
ENST00000682303.1:c.*2914G>A
|
ENSP00000508325.1:n.*2914G>A
|
|
ENST00000682308.1:c.3128G>A
|
ENSP00000507056.1:p.Cys1043Tyr
|
|
ENST00000682480.1:c.3146G>A
|
ENSP00000508344.1:p.Cys1049Tyr
|
|
ENST00000682546.1:c.3125G>A
|
ENSP00000508188.1:p.Cys1042Tyr
|
|
ENST00000682585.1:c.3128G>A
|
ENSP00000506885.1:p.Cys1043Tyr
|
|
ENST00000682595.1:n.3712G>A
|
|
|
ENST00000682607.1:c.1546G>A
|
|
|
ENST00000682779.1:c.3119G>A
|
ENSP00000507947.1:p.Cys1040Tyr
|
|
ENST00000682845.1:n.2230G>A
|
|
|
ENST00000682885.1:c.3083G>A
|
ENSP00000508036.1:p.Cys1028Tyr
|
|
ENST00000682933.1:n.3202G>A
|
|
|
ENST00000683072.1:n.3712G>A
|
|
|
ENST00000683080.1:n.747G>A
|
|
|
ENST00000683125.1:c.3236G>A
|
ENSP00000507939.1:p.Cys1079Tyr
|
|
ENST00000683213.1:c.3131G>A
|
ENSP00000507751.1:p.Cys1044Tyr
|
|
ENST00000683220.1:c.3158G>A
|
ENSP00000507151.1:p.Cys1053Tyr
|
|
ENST00000683329.1:n.3931G>A
|
|
|
ENST00000683346.1:c.*3003G>A
|
ENSP00000507458.1:n.*3003G>A
|
|
ENST00000683409.1:n.1735G>A
|
|
|
ENST00000683459.1:n.3715G>A
|
|
|
ENST00000683590.1:c.2897-5487G>A
|
ENSP00000506820.1:n.2897-5487G>A
|
|
ENST00000683623.1:c.3035G>A
|
ENSP00000507702.1:p.Cys1012Tyr
|
|
ENST00000683645.1:n.3679G>A
|
|
|
ENST00000683796.1:c.*3000G>A
|
ENSP00000508221.1:n.*3000G>A
|
|
ENST00000683802.1:n.6053G>A
|
|
|
ENST00000683833.1:c.3119G>A
|
ENSP00000506852.1:p.Cys1040Tyr
|
|
ENST00000683994.1:c.3128G>A
|
ENSP00000507181.1:p.Cys1043Tyr
|
|
ENST00000684290.1:c.*664G>A
|
ENSP00000507243.1:n.*664G>A
|
|
ENST00000684306.1:c.*3041G>A
|
ENSP00000508384.1:n.*3041G>A
|
|
ENST00000684341.1:n.3148G>A
|
|
|
ENST00000684383.1:c.*2766G>A
|
ENSP00000506863.1:n.*2766G>A
|
|
ENST00000684619.1:c.*3000G>A
|
ENSP00000508088.1:n.*3000G>A
|
|
ENST00000684705.1:n.249G>A
|
|
|
ENST00000684743.1:n.4159G>A
|
|
|
ENST00000260665.12:c.3128G>A
MANE Select
|
ENSP00000260665.7:p.Cys1043Tyr
|
|
ENST00000260665.11:c.3128G>A
|
ENSP00000260665.7:p.Cys1043Tyr
|
|
NM_133259.3:c.3128G>A
|
NP_573566.2:p.Cys1043Tyr
|
|
XM_006711915.2:c.3050G>A
|
XP_006711978.1:p.Cys1017Tyr
|
|
XM_006711916.2:c.3128G>A
|
XP_006711979.1:p.Cys1043Tyr
|
|
XM_011532473.1:c.3128G>A
|
XP_011530775.1:p.Cys1043Tyr
|
|
XM_011532474.1:c.3128G>A
|
XP_011530776.1:p.Cys1043Tyr
|
|
XM_006711916.3:c.3128G>A
|
XP_006711979.1:p.Cys1043Tyr
|
|
XM_017003117.1:c.3050G>A
|
XP_016858606.1:p.Cys1017Tyr
|
|
XR_002958896.1:n.3170G>A
|
|
|
NM_133259.4:c.3128G>A
MANE Select
|
NP_573566.2:p.Cys1043Tyr
|
|