ENST00000324856.13:c.5309G=
MANE Select
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ENSP00000320485.7:p.Gly1770=
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ENST00000374152.7:c.4160G=
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ENSP00000363267.2:p.Gly1387=
|
|
ENST00000430799.7:c.4157G=
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ENSP00000390317.3:p.Gly1386=
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ENST00000466382.2:c.726G=
|
|
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ENST00000636219.1:c.4163G=
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ENSP00000489842.1:p.Gly1388=
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ENST00000637788.1:n.1109G=
|
|
|
ENST00000324856.11:c.5309G=
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ENSP00000320485.7:p.Gly1770=
|
|
ENST00000374152.6:c.4160G=
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ENSP00000363267.2:p.Gly1387=
|
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ENST00000430799.6:c.1998G=
|
|
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ENST00000457599.6:c.4658G=
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ENSP00000387636.2:p.Gly1553=
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ENST00000466382.1:c.726G=
|
|
|
ENST00000532781.1:c.807G=
|
|
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NM_006015.4:c.5309G= , LRG_875t1:c.5309G=
|
NP_006006.3:p.Gly1770=
|
|
NM_139135.2:c.4658G=
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NP_624361.1:p.Gly1553=
|
|
NM_006015.5:c.5309G=
|
NP_006006.3:p.Gly1770=
|
|
NM_139135.3:c.4658G=
|
NP_624361.1:p.Gly1553=
|
|
NM_006015.6:c.5309G=
MANE Select
|
NP_006006.3:p.Gly1770=
|
|
NM_139135.4:c.4658G=
|
NP_624361.1:p.Gly1553=
|
|