ENST00000324856.13:c.5282G=
MANE Select
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ENSP00000320485.7:p.Gly1761=
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ENST00000374152.7:c.4133G=
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ENSP00000363267.2:p.Gly1378=
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ENST00000430799.7:c.4130G=
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ENSP00000390317.3:p.Gly1377=
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ENST00000466382.2:c.699G=
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|
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ENST00000636219.1:c.4136G=
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ENSP00000489842.1:p.Gly1379=
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ENST00000637788.1:n.1082G=
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|
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ENST00000324856.11:c.5282G=
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ENSP00000320485.7:p.Gly1761=
|
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ENST00000374152.6:c.4133G=
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ENSP00000363267.2:p.Gly1378=
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ENST00000430799.6:c.1971G=
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|
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ENST00000457599.6:c.4631G=
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ENSP00000387636.2:p.Gly1544=
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ENST00000466382.1:c.699G=
|
|
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ENST00000532781.1:c.780G=
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|
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NM_006015.4:c.5282G= , LRG_875t1:c.5282G=
|
NP_006006.3:p.Gly1761=
|
|
NM_139135.2:c.4631G=
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NP_624361.1:p.Gly1544=
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NM_006015.5:c.5282G=
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NP_006006.3:p.Gly1761=
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|
NM_139135.3:c.4631G=
|
NP_624361.1:p.Gly1544=
|
|
NM_006015.6:c.5282G=
MANE Select
|
NP_006006.3:p.Gly1761=
|
|
NM_139135.4:c.4631G=
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NP_624361.1:p.Gly1544=
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