|
ENST00000374647.10:c.2817C>G
MANE Select
|
ENSP00000363779.5:p.Tyr939Ter
|
|
|
ENST00000495759.6:c.*1427C>G
|
ENSP00000433514.2:n.*1427C>G
|
|
|
ENST00000674535.1:c.2817C>G
|
ENSP00000502142.1:p.Tyr939Ter
|
|
|
ENST00000674704.1:n.5902C>G
|
|
|
|
ENST00000674836.1:n.3430C>G
|
|
|
|
ENST00000674890.1:c.*52C>G
|
ENSP00000501870.1:n.*52C>G
|
|
|
ENST00000674938.1:c.2475C>G
|
ENSP00000502427.1:p.Tyr825Ter
|
|
|
ENST00000674948.1:c.2475C>G
|
ENSP00000501602.1:p.Tyr825Ter
|
|
|
ENST00000675052.1:c.2817C>G
|
ENSP00000502664.1:p.Tyr939Ter
|
|
|
ENST00000675078.1:c.2817C>G
|
ENSP00000501549.1:p.Tyr939Ter
|
|
|
ENST00000675215.1:c.*2041C>G
|
ENSP00000502558.1:n.*2041C>G
|
|
|
ENST00000675233.1:n.4644C>G
|
|
|
|
ENST00000675321.1:c.2817C>G
|
ENSP00000502751.1:p.Tyr939Ter
|
|
|
ENST00000675325.1:n.4774C>G
|
|
|
|
ENST00000675335.1:c.2848C>G
|
ENSP00000502182.1:n.2848C>G
|
|
|
ENST00000675400.1:n.4552C>G
|
|
|
|
ENST00000675406.1:c.2817C>G
|
ENSP00000501893.1:p.Tyr939Ter
|
|
|
ENST00000675458.1:c.2910C>G
|
ENSP00000501754.1:n.2910C>G
|
|
|
ENST00000675507.1:n.4613C>G
|
|
|
|
ENST00000675535.1:c.*444C>G
|
ENSP00000501667.1:n.*444C>G
|
|
|
ENST00000675566.1:n.4675C>G
|
|
|
|
ENST00000675602.1:n.5865C>G
|
|
|
|
ENST00000675647.1:n.3122C>G
|
|
|
|
ENST00000675711.1:c.2817C>G
|
ENSP00000502485.1:p.Tyr939Ter
|
|
|
ENST00000675727.1:c.2817C>G
|
ENSP00000501722.1:p.Tyr939Ter
|
|
|
ENST00000675748.1:n.4451C>G
|
|
|
|
ENST00000675765.1:c.*200C>G
|
ENSP00000502640.1:n.*200C>G
|
|
|
ENST00000675825.1:c.2817C>G
|
ENSP00000502632.1:p.Tyr939Ter
|
|
|
ENST00000675877.1:n.3122C>G
|
|
|
|
ENST00000675893.1:c.*3886C>G
|
ENSP00000502001.1:n.*3886C>G
|
|
|
ENST00000675943.1:n.6432C>G
|
|
|
|
ENST00000675979.1:c.*2060C>G
|
ENSP00000502208.1:n.*2060C>G
|
|
|
ENST00000676044.1:c.*477C>G
|
ENSP00000502378.1:n.*477C>G
|
|
|
ENST00000676086.1:n.4602C>G
|
|
|
|
ENST00000676121.1:n.4645C>G
|
|
|
|
ENST00000676237.1:c.2718C>G
|
ENSP00000501828.1:p.Tyr906Ter
|
|
|
ENST00000676416.1:c.2475C>G
|
ENSP00000501660.1:p.Tyr825Ter
|
|
|
ENST00000676424.1:n.4613C>G
|
|
|
|
ENST00000676429.1:n.7286C>G
|
|
|
|
ENST00000374647.9:c.2817C>G
|
ENSP00000363779.5:p.Tyr939Ter
|
|
|
ENST00000537196.1:c.1770C>G
|
ENSP00000439367.1:p.Tyr590Ter
|
|
|
NM_003640.3:c.2817C>G , LRG_251t1:c.2817C>G
|
NP_003631.2:p.Tyr939Ter
|
|
|
XM_005252285.2:c.2475C>G
|
XP_005252342.1:p.Tyr825Ter
|
|
|
XM_011519136.1:c.2817C>G
|
XP_011517438.1:p.Tyr939Ter
|
|
|
XM_011519137.1:c.2475C>G
|
XP_011517439.1:p.Tyr825Ter
|
|
|
XR_929859.1:n.3195C>G
|
|
|
|
NM_001318360.1:c.2475C>G
|
NP_001305289.1:p.Tyr825Ter
|
|
|
NM_001330749.1:c.1770C>G
|
NP_001317678.1:p.Tyr590Ter
|
|
|
NM_003640.4:c.2817C>G
|
NP_003631.2:p.Tyr939Ter
|
|
|
XM_011519136.2:c.2817C>G
|
XP_011517438.1:p.Tyr939Ter
|
|
|
XR_929859.3:n.3206C>G
|
|
|
|
NM_003640.5:c.2817C>G
MANE Select
|
NP_003631.2:p.Tyr939Ter
|
|
|
NM_001318360.2:c.2475C>G
|
NP_001305289.1:p.Tyr825Ter
|
|
|
NM_001330749.2:c.1770C>G
|
NP_001317678.1:p.Tyr590Ter
|
|
