ENST00000260983.8:c.2581C>T
|
ENSP00000260983.2:p.Arg861Trp
|
|
ENST00000644030.1:c.2602C>T
|
ENSP00000495504.1:p.Arg868Trp
|
|
ENST00000644256.1:c.2581C>T
|
ENSP00000494649.1:p.Arg861Trp
|
|
ENST00000644405.1:n.218C>T
|
|
|
ENST00000644421.1:c.389C>T
|
|
|
ENST00000644978.2:c.2581C>T
MANE Select
|
ENSP00000495418.1:p.Arg861Trp
|
|
ENST00000647236.1:c.*1767C>T
|
ENSP00000494800.1:n.*1767C>T
|
|
ENST00000260983.7:c.2581C>T
|
ENSP00000260983.2:p.Arg861Trp
|
|
ENST00000409111.2:c.1513C>T
|
ENSP00000386775.1:p.Arg505Trp
|
|
NM_001304840.1:c.1513C>T
|
NP_001291769.1:p.Arg505Trp
|
|
NM_020760.2:c.2581C>T
|
NP_065811.1:p.Arg861Trp
|
|
XM_006712646.2:c.2602C>T
|
XP_006712709.1:p.Arg868Trp
|
|
XM_006712648.2:c.2209C>T
|
XP_006712711.1:p.Arg737Trp
|
|
NM_001304840.2:c.1513C>T
|
NP_001291769.1:p.Arg505Trp
|
|
NM_001348768.1:c.2581C>T
|
NP_001335697.1:p.Arg861Trp
|
|
NM_020760.3:c.2581C>T
|
NP_065811.1:p.Arg861Trp
|
|
XM_006712646.3:c.2602C>T
|
XP_006712709.1:p.Arg868Trp
|
|
XM_006712648.4:c.2209C>T
|
XP_006712711.1:p.Arg737Trp
|
|
XM_024453020.1:c.2602C>T
|
XP_024308788.1:p.Arg868Trp
|
|
XM_024453021.1:c.2602C>T
|
XP_024308789.1:p.Arg868Trp
|
|
NM_001348768.2:c.2581C>T
MANE Select
|
NP_001335697.1:p.Arg861Trp
|
|
NM_001304840.3:c.1513C>T
|
NP_001291769.1:p.Arg505Trp
|
|
NM_020760.4:c.2581C>T
|
NP_065811.1:p.Arg861Trp
|
|