|
ENST00000681993.1:n.600T=
|
|
|
|
ENST00000682295.1:c.303+131T=
|
ENSP00000507499.1:n.303+131T=
|
|
|
ENST00000682303.1:c.*2834T=
|
ENSP00000508325.1:n.*2834T=
|
|
|
ENST00000682308.1:c.3048T=
|
ENSP00000507056.1:p.Tyr1016=
|
|
|
ENST00000682480.1:c.3066T=
|
ENSP00000508344.1:p.Tyr1022=
|
|
|
ENST00000682546.1:c.3045T=
|
ENSP00000508188.1:p.Tyr1015=
|
|
|
ENST00000682585.1:c.3048T=
|
ENSP00000506885.1:p.Tyr1016=
|
|
|
ENST00000682595.1:n.3632T=
|
|
|
|
ENST00000682607.1:c.1466T=
|
|
|
|
ENST00000682779.1:c.3039T=
|
ENSP00000507947.1:p.Tyr1013=
|
|
|
ENST00000682845.1:n.2150T=
|
|
|
|
ENST00000682885.1:c.3003T=
|
ENSP00000508036.1:p.Tyr1001=
|
|
|
ENST00000682933.1:n.3122T=
|
|
|
|
ENST00000683072.1:n.3632T=
|
|
|
|
ENST00000683080.1:n.667T=
|
|
|
|
ENST00000683125.1:c.3156T=
|
ENSP00000507939.1:p.Tyr1052=
|
|
|
ENST00000683213.1:c.3051T=
|
ENSP00000507751.1:p.Tyr1017=
|
|
|
ENST00000683220.1:c.3078T=
|
ENSP00000507151.1:p.Tyr1026=
|
|
|
ENST00000683329.1:n.3851T=
|
|
|
|
ENST00000683346.1:c.*2923T=
|
ENSP00000507458.1:n.*2923T=
|
|
|
ENST00000683409.1:n.1655T=
|
|
|
|
ENST00000683459.1:n.3635T=
|
|
|
|
ENST00000683590.1:c.2897-5567T=
|
ENSP00000506820.1:n.2897-5567T=
|
|
|
ENST00000683623.1:c.2955T=
|
ENSP00000507702.1:p.Tyr985=
|
|
|
ENST00000683645.1:n.3599T=
|
|
|
|
ENST00000683796.1:c.*2920T=
|
ENSP00000508221.1:n.*2920T=
|
|
|
ENST00000683802.1:n.5973T=
|
|
|
|
ENST00000683833.1:c.3039T=
|
ENSP00000506852.1:p.Tyr1013=
|
|
|
ENST00000683994.1:c.3048T=
|
ENSP00000507181.1:p.Tyr1016=
|
|
|
ENST00000684290.1:c.*584T=
|
ENSP00000507243.1:n.*584T=
|
|
|
ENST00000684306.1:c.*2961T=
|
ENSP00000508384.1:n.*2961T=
|
|
|
ENST00000684341.1:n.3068T=
|
|
|
|
ENST00000684383.1:c.*2686T=
|
ENSP00000506863.1:n.*2686T=
|
|
|
ENST00000684619.1:c.*2920T=
|
ENSP00000508088.1:n.*2920T=
|
|
|
ENST00000684705.1:n.169T=
|
|
|
|
ENST00000684743.1:n.4079T=
|
|
|
|
ENST00000260665.12:c.3048T=
MANE Select
|
ENSP00000260665.7:p.Tyr1016=
|
|
|
ENST00000260665.11:c.3048T=
|
ENSP00000260665.7:p.Tyr1016=
|
|
|
NM_133259.3:c.3048T=
|
NP_573566.2:p.Tyr1016=
|
|
|
XM_006711915.2:c.2970T=
|
XP_006711978.1:p.Tyr990=
|
|
|
XM_006711916.2:c.3048T=
|
XP_006711979.1:p.Tyr1016=
|
|
|
XM_011532473.1:c.3048T=
|
XP_011530775.1:p.Tyr1016=
|
|
|
XM_011532474.1:c.3048T=
|
XP_011530776.1:p.Tyr1016=
|
|
|
XM_006711916.3:c.3048T=
|
XP_006711979.1:p.Tyr1016=
|
|
|
XM_017003117.1:c.2970T=
|
XP_016858606.1:p.Tyr990=
|
|
|
XR_002958896.1:n.3090T=
|
|
|
|
NM_133259.4:c.3048T=
MANE Select
|
NP_573566.2:p.Tyr1016=
|
|
