ENST00000600737.6:c.3734G>T
MANE Select
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ENSP00000473211.1:p.Gly1245Val
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ENST00000221249.10:c.3620G>T
|
ENSP00000221249.5:p.Gly1207Val
|
|
ENST00000414982.7:c.3764G>T
|
ENSP00000407509.2:p.Gly1255Val
|
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ENST00000450331.7:c.3620G>T
|
ENSP00000394348.2:p.Gly1207Val
|
|
ENST00000545201.6:c.3539G>T
|
ENSP00000443323.1:p.Gly1180Val
|
|
ENST00000597202.1:n.92G>T
|
|
|
ENST00000599947.1:c.186-332G>T
|
|
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ENST00000600737.5:c.3734G>T
|
ENSP00000473211.1:p.Gly1245Val
|
|
NM_001166111.1:c.3764G>T
|
NP_001159583.1:p.Gly1255Val
|
|
NM_001166112.1:c.3539G>T
|
NP_001159584.1:p.Gly1180Val
|
|
NM_001166113.1:c.3620G>T
|
NP_001159585.1:p.Gly1207Val
|
|
NM_001166114.1:c.3734G>T
|
NP_001159586.1:p.Gly1245Val
|
|
NM_006702.4:c.3620G>T
|
NP_006693.3:p.Gly1207Val
|
|
NM_001166111.2:c.3764G>T
|
NP_001159583.1:p.Gly1255Val
|
|
NM_001166114.2:c.3734G>T
MANE Select
|
NP_001159586.1:p.Gly1245Val
|
|
NM_006702.5:c.3620G>T
|
NP_006693.3:p.Gly1207Val
|
|
NM_001166112.2:c.3539G>T
|
NP_001159584.1:p.Gly1180Val
|
|