ENST00000600737.6:c.3897T>C
MANE Select
|
ENSP00000473211.1:p.Ser1299=
|
|
ENST00000221249.10:c.3783T>C
|
ENSP00000221249.5:p.Ser1261=
|
|
ENST00000414982.7:c.3927T>C
|
ENSP00000407509.2:p.Ser1309=
|
|
ENST00000450331.7:c.3783T>C
|
ENSP00000394348.2:p.Ser1261=
|
|
ENST00000545201.6:c.3702T>C
|
ENSP00000443323.1:p.Ser1234=
|
|
ENST00000597202.1:n.255T>C
|
|
|
ENST00000599947.1:c.266T>C
|
|
|
ENST00000600737.5:c.3897T>C
|
ENSP00000473211.1:p.Ser1299=
|
|
NM_001166111.1:c.3927T>C
|
NP_001159583.1:p.Ser1309=
|
|
NM_001166112.1:c.3702T>C
|
NP_001159584.1:p.Ser1234=
|
|
NM_001166113.1:c.3783T>C
|
NP_001159585.1:p.Ser1261=
|
|
NM_001166114.1:c.3897T>C
|
NP_001159586.1:p.Ser1299=
|
|
NM_006702.4:c.3783T>C
|
NP_006693.3:p.Ser1261=
|
|
NM_001166111.2:c.3927T>C
|
NP_001159583.1:p.Ser1309=
|
|
NM_001166114.2:c.3897T>C
MANE Select
|
NP_001159586.1:p.Ser1299=
|
|
NM_006702.5:c.3783T>C
|
NP_006693.3:p.Ser1261=
|
|
NM_001166112.2:c.3702T>C
|
NP_001159584.1:p.Ser1234=
|
|