ENST00000322213.9:c.1842C=
MANE Select
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ENSP00000323421.3:p.Gly614=
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ENST00000674590.1:c.1074C=
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ENSP00000502626.1:p.Gly358=
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ENST00000675065.1:n.1194C=
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|
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ENST00000675504.1:c.1776C=
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ENSP00000502524.1:p.Gly592=
|
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ENST00000322213.8:c.1842C=
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ENSP00000323421.3:p.Gly614=
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ENST00000375340.10:c.1776C=
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ENSP00000364489.7:p.Gly592=
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NM_001281463.1:c.1776C= , LRG_773t1:c.1776C=
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NP_001268392.1:p.Gly592=
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NM_006306.3:c.1842C= , LRG_773t2:c.1842C=
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NP_006297.2:p.Gly614=
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NM_006306.4:c.1842C=
MANE Select
|
NP_006297.2:p.Gly614=
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