ENST00000698234.1:n.1418G>A
|
|
|
ENST00000698317.1:n.2034G>A
|
|
|
ENST00000698318.1:n.1817G>A
|
|
|
ENST00000698319.1:n.1180G>A
|
|
|
ENST00000698320.1:n.1068G>A
|
|
|
ENST00000470127.2:n.1081G>A
|
|
|
ENST00000475699.6:c.572G>A
|
ENSP00000419854.3:p.Cys191Tyr
|
|
ENST00000483674.3:n.490G>A
|
|
|
ENST00000601016.6:c.608G>A
MANE Select
|
ENSP00000469981.1:p.Cys203Tyr
|
|
ENST00000612012.5:c.566G>A
|
ENSP00000482070.2:p.Cys189Tyr
|
|
ENST00000612460.5:c.518G>A
|
ENSP00000481037.1:p.Cys173Tyr
|
|
ENST00000614595.2:n.1955G>A
|
|
|
ENST00000615658.5:n.1197G>A
|
|
|
ENST00000616020.5:c.620G>A
|
ENSP00000483636.2:p.Cys207Tyr
|
|
ENST00000617701.5:c.*621G>A
|
ENSP00000481645.1:n.*621G>A
|
|
ENST00000652354.1:c.290G>A
|
ENSP00000498734.1:p.Cys97Tyr
|
|
ENST00000652358.1:c.401G>A
|
ENSP00000498464.1:p.Cys134Tyr
|
|
ENST00000652390.1:c.527G>A
|
ENSP00000498858.1:p.Cys176Tyr
|
|
ENST00000652476.1:n.1274G>A
|
|
|
ENST00000652644.1:c.221G>A
|
ENSP00000498496.1:p.Cys74Tyr
|
|
ENST00000652682.1:c.665G>A
|
ENSP00000498288.1:p.Cys222Tyr
|
|
ENST00000652685.1:n.961G>A
|
|
|
ENST00000369776.8:c.401G>A
|
ENSP00000358791.4:p.Cys134Tyr
|
|
ENST00000426231.5:c.605G>A
|
|
|
ENST00000439735.2:c.515G>A
|
ENSP00000398193.1:p.Cys172Tyr
|
|
ENST00000470127.1:n.187G>A
|
|
|
ENST00000475699.5:c.566G>A
|
ENSP00000419854.2:p.Cys189Tyr
|
|
ENST00000494912.5:n.1297G>A
|
|
|
ENST00000498029.1:n.66G>A
|
|
|
ENST00000601016.5:c.608G>A
|
ENSP00000469981.1:p.Cys203Tyr
|
|
ENST00000612012.4:c.572G>A
|
ENSP00000482070.1:p.Cys191Tyr
|
|
ENST00000612460.4:c.518G>A
|
ENSP00000481037.1:p.Cys173Tyr
|
|
ENST00000613002.4:c.476G>A
|
ENSP00000478154.1:p.Cys159Tyr
|
|
ENST00000615658.4:n.1297G>A
|
|
|
ENST00000615986.4:c.*336G>A
|
ENSP00000480133.1:n.*336G>A
|
|
ENST00000620808.4:c.*194G>A
|
ENSP00000479311.1:n.*194G>A
|
|
NM_000116.4:c.608G>A
|
NP_000107.1:p.Cys203Tyr
|
|
NM_001303465.1:c.620G>A
|
NP_001290394.1:p.Cys207Tyr
|
|
NM_181311.3:c.518G>A
|
NP_851828.1:p.Cys173Tyr
|
|
NM_181312.3:c.566G>A
|
NP_851829.1:p.Cys189Tyr
|
|
NM_181313.3:c.476G>A
|
NP_851830.1:p.Cys159Tyr
|
|
NR_024048.2:n.950G>A
|
|
|
XM_006724836.1:c.662G>A
|
XP_006724899.1:p.Cys221Tyr
|
|
XM_006724837.1:c.530G>A
|
XP_006724900.1:p.Cys177Tyr
|
|
XM_006724839.1:c.530G>A
|
XP_006724902.1:p.Cys177Tyr
|
|
XM_006724841.2:c.401G>A
|
XP_006724904.1:p.Cys134Tyr
|
|
XM_006724842.2:c.311G>A
|
XP_006724905.1:p.Cys104Tyr
|
|
XM_011531189.1:c.449G>A
|
XP_011529491.1:p.Cys150Tyr
|
|
XM_011531190.1:c.401G>A
|
XP_011529492.1:p.Cys134Tyr
|
|
XM_011531191.1:c.332G>A
|
XP_011529493.1:p.Cys111Tyr
|
|
XM_011531192.1:c.329G>A
|
XP_011529494.1:p.Cys110Tyr
|
|
XR_938511.1:n.956G>A
|
|
|
XM_006724841.4:c.401G>A
|
XP_006724904.1:p.Cys134Tyr
|
|
XM_006724842.4:c.311G>A
|
XP_006724905.1:p.Cys104Tyr
|
|
XM_011531191.2:c.332G>A
|
XP_011529493.1:p.Cys111Tyr
|
|
XM_017029761.1:c.476G>A
|
XP_016885250.1:p.Cys159Tyr
|
|
XM_017029762.1:c.572G>A
|
XP_016885251.1:p.Cys191Tyr
|
|
XM_017029763.1:c.395G>A
|
XP_016885252.1:p.Cys132Tyr
|
|
XM_017029764.1:c.329G>A
|
XP_016885253.1:p.Cys110Tyr
|
|
XM_017029765.2:c.269G>A
|
XP_016885254.1:p.Cys90Tyr
|
|
XM_024452431.1:c.449G>A
|
XP_024308199.1:p.Cys150Tyr
|
|
NM_000116.5:c.608G>A
MANE Select
|
NP_000107.1:p.Cys203Tyr
|
|
NM_001303465.2:c.620G>A
|
NP_001290394.1:p.Cys207Tyr
|
|
NM_181311.4:c.518G>A
|
NP_851828.1:p.Cys173Tyr
|
|
NM_181312.4:c.566G>A
|
NP_851829.1:p.Cys189Tyr
|
|
NM_181313.4:c.476G>A
|
NP_851830.1:p.Cys159Tyr
|
|
NR_024048.3:n.929G>A
|
|
|