|
NM_003060.4:c.1161T>G
MANE Select
|
NP_003051.1:p.Tyr387Ter
|
|
ENST00000245407.8:c.1161T>G
MANE Select
|
ENSP00000245407.3:p.Tyr387Ter
|
|
NM_001308122.1:c.1233T>G
|
NP_001295051.1:p.Tyr411Ter
|
|
NM_001308122.2:c.1233T>G
|
NP_001295051.1:p.Tyr411Ter
|
|
NM_003060.3:c.1161T>G
|
NP_003051.1:p.Tyr387Ter
|
|
ENST00000245407.7:c.1161T>G
|
ENSP00000245407.3:p.Tyr387Ter
|
|
ENST00000415928.6:c.1002T>G
|
ENSP00000388838.2:p.Tyr334Ter
|
|
ENST00000435065.6:c.1233T>G
|
ENSP00000402760.2:p.Tyr411Ter
|
|
ENST00000435065.7:c.1233T>G
|
ENSP00000402760.2:p.Tyr411Ter
|
|
ENST00000447841.5:c.112-1635T>G
|
|
|
ENST00000448810.5:c.423T>G
|
|
|
ENST00000448810.6:c.*13T>G
|
ENSP00000401860.2:n.*13T>G
|
|
ENST00000461013.5:n.8583T>G
|
|
|
ENST00000475308.1:n.1839T>G
|
|
|
ENST00000479605.5:n.264T>G
|
|
|
ENST00000685543.1:n.1302T>G
|
|
|
ENST00000686757.1:c.*325T>G
|
ENSP00000510721.1:n.*325T>G
|
|
ENST00000687740.1:n.3846T>G
|
|
|
ENST00000688151.1:n.2471T>G
|
|
|
ENST00000689271.1:c.1008T>G
|
ENSP00000510797.1:p.Tyr336Ter
|
|
ENST00000690900.1:c.*325T>G
|
ENSP00000510703.1:n.*325T>G
|
|
ENST00000692212.1:n.2773T>G
|
|
|
ENST00000692355.1:c.414T>G
|
|
|
ENST00000692413.1:c.1143T>G
|
ENSP00000509374.1:p.Tyr381Ter
|
|
ENST00000692825.1:c.1229T>G
|
ENSP00000509447.1:n.1229T>G
|
|
ENST00000693308.1:c.1209T>G
|
ENSP00000509770.1:p.Tyr403Ter
|
|
ENST00000693763.1:n.2321T>G
|
|
|
XM_011543590.1:c.543T>G
|
XP_011541892.1:p.Tyr181Ter
|
|
XM_011543590.2:c.543T>G
|
XP_011541892.1:p.Tyr181Ter
|
|
XM_017009778.2:c.633T>G
|
XP_016865267.1:p.Tyr211Ter
|
|
XR_001742215.1:n.1416T>G
|
|
|
XR_001742216.1:n.1435T>G
|
|
|
XR_427718.1:n.1521T>G
|
|
|
XR_427718.2:n.1521T>G
|
|
|
XR_948290.1:n.1394-1635T>G
|
|
|
XR_948290.2:n.1394-1635T>G
|
|
|
XR_948291.1:n.1515T>G
|
|
|
XR_948291.2:n.1515T>G
|
|
