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ENST00000360822.8:c.2941T=
|
ENSP00000354065.4:p.Tyr981=
|
|
|
ENST00000416449.6:c.3535T=
|
ENSP00000400395.2:p.Tyr1179=
|
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ENST00000479584.2:n.1878T=
|
|
|
|
ENST00000684780.1:n.3921T=
|
|
|
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ENST00000685866.1:c.*1458T=
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ENSP00000509484.1:n.*1458T=
|
|
|
ENST00000686376.1:c.3711T=
|
ENSP00000510021.1:n.3711T=
|
|
|
ENST00000686842.1:n.7185T=
|
|
|
|
ENST00000687279.1:c.3628T=
|
ENSP00000508692.1:p.Tyr1210=
|
|
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ENST00000687311.1:n.3594T=
|
|
|
|
ENST00000687633.1:c.3532T=
|
ENSP00000510289.1:p.Tyr1178=
|
|
|
ENST00000688923.1:n.3003T=
|
|
|
|
ENST00000689688.1:c.3631T=
|
ENSP00000510155.1:p.Tyr1211=
|
|
|
ENST00000690646.1:c.3535T=
|
ENSP00000510383.1:p.Tyr1179=
|
|
|
ENST00000690814.1:c.*807T=
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ENSP00000508792.1:n.*807T=
|
|
|
ENST00000691504.1:n.3525T=
|
|
|
|
ENST00000692155.1:c.3711T=
|
ENSP00000510290.1:n.3711T=
|
|
|
ENST00000692746.1:n.3538T=
|
|
|
|
ENST00000693386.1:c.3535T=
|
ENSP00000510003.1:p.Tyr1179=
|
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ENST00000693433.1:n.3525T=
|
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ENST00000693714.1:n.3578T=
|
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|
ENST00000693728.1:c.3535T=
|
ENSP00000510580.1:p.Tyr1179=
|
|
|
ENST00000349780.9:c.3631T=
MANE Select
|
ENSP00000343818.4:p.Tyr1211=
|
|
|
ENST00000349780.8:c.3631T=
|
ENSP00000343818.4:p.Tyr1211=
|
|
|
ENST00000360190.8:c.3631T=
|
ENSP00000353317.4:p.Tyr1211=
|
|
|
ENST00000360822.7:c.2941T=
|
ENSP00000354065.4:p.Tyr981=
|
|
|
ENST00000416449.5:c.1813T=
|
ENSP00000400395.1:p.Tyr605=
|
|
|
ENST00000425647.1:c.661T=
|
ENSP00000409941.1:p.Tyr221=
|
|
|
ENST00000473282.6:c.*2455T=
|
ENSP00000419265.1:n.*2455T=
|
|
|
ENST00000480112.5:c.*1458T=
|
ENSP00000418418.1:n.*1458T=
|
|
|
ENST00000483412.5:n.2939T=
|
|
|
|
NM_001011649.2:c.3631T=
|
NP_001011649.1:p.Tyr1211=
|
|
|
NM_001272039.1:c.2941T=
|
NP_001258968.1:p.Tyr981=
|
|
|
NM_018249.5:c.3631T=
|
NP_060719.4:p.Tyr1211=
|
|
|
NR_073554.1:n.3900T=
|
|
|
|
NR_073555.1:n.3823T=
|
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NR_073556.1:n.4030T=
|
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NR_073557.1:n.3903T=
|
|
|
|
NR_073558.1:n.3900T=
|
|
|
|
XM_006717182.1:c.3535T=
|
XP_006717245.1:p.Tyr1179=
|
|
|
XM_006717185.1:c.2944T=
|
XP_006717248.1:p.Tyr982=
|
|
|
XM_011518860.1:c.3628T=
|
XP_011517162.1:p.Tyr1210=
|
|
|
XM_011518861.1:c.3628T=
|
XP_011517163.1:p.Tyr1210=
|
|
|
XM_017014921.1:c.3532T=
|
XP_016870410.1:p.Tyr1178=
|
|
|
XM_017014922.1:c.2797T=
|
XP_016870411.1:p.Tyr933=
|
|
|
XM_017014923.1:c.2944T=
|
XP_016870412.1:p.Tyr982=
|
|
|
XM_017014924.1:c.1426T=
|
XP_016870413.1:p.Tyr476=
|
|
|
NM_018249.6:c.3631T=
MANE Select
|
NP_060719.4:p.Tyr1211=
|
|
|
NM_001011649.3:c.3631T=
|
NP_001011649.1:p.Tyr1211=
|
|
|
NR_073554.2:n.3897T=
|
|
|
|
NR_073555.2:n.3820T=
|
|
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|
NR_073556.2:n.4027T=
|
|
|
|
NR_073557.2:n.3900T=
|
|
|
|
NR_073558.2:n.3897T=
|
|
|
|
NM_001272039.2:c.2941T=
|
NP_001258968.1:p.Tyr981=
|
|
