ENST00000261304.7:c.1481T>A
MANE Select
|
ENSP00000261304.2:p.Phe494Tyr
|
|
ENST00000261304.6:c.1481T>A
|
ENSP00000261304.2:p.Phe494Tyr
|
|
ENST00000393568.8:c.1412T>A
|
ENSP00000377198.4:p.Phe471Tyr
|
|
ENST00000393569.6:c.1403T>A
|
ENSP00000377199.2:p.Phe468Tyr
|
|
ENST00000544807.6:c.1313T>A
|
ENSP00000437513.2:p.Phe438Tyr
|
|
ENST00000555000.5:c.848T>A
|
ENSP00000450472.1:p.Phe283Tyr
|
|
ENST00000555179.1:c.198T>A
|
|
|
ENST00000557316.5:c.*879T>A
|
ENSP00000452314.1:n.*879T>A
|
|
NM_000153.3:c.1481T>A
|
NP_000144.2:p.Phe494Tyr
|
|
NM_001201401.1:c.1412T>A
|
NP_001188330.1:p.Phe471Tyr
|
|
NM_001201402.1:c.1403T>A
|
NP_001188331.1:p.Phe468Tyr
|
|
XM_011536618.1:c.1313T>A
|
XP_011534920.1:p.Phe438Tyr
|
|
XM_011536618.2:c.1313T>A
|
XP_011534920.1:p.Phe438Tyr
|
|
NM_000153.4:c.1481T>A
MANE Select
|
NP_000144.2:p.Phe494Tyr
|
|
NM_001201401.2:c.1412T>A
|
NP_001188330.1:p.Phe471Tyr
|
|
NM_001201402.2:c.1403T>A
|
NP_001188331.1:p.Phe468Tyr
|
|