ENST00000394867.9:n.1610C>G
|
|
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ENST00000688002.1:n.3322C>G
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|
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ENST00000688751.1:n.307C>G
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|
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ENST00000689792.1:n.1075C>G
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|
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ENST00000262948.10:c.1171C>G
MANE Select
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ENSP00000262948.4:p.Gln391Glu
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ENST00000262948.9:c.1171C>G
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ENSP00000262948.3:p.Gln391Glu
|
|
ENST00000394867.8:c.880C>G
|
ENSP00000378336.1:p.Gln294Glu
|
|
ENST00000597263.5:n.356C>G
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|
|
ENST00000599021.1:c.281C>G
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|
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ENST00000600584.5:n.2620C>G
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|
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ENST00000601786.5:n.1472C>G
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|
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NM_030662.3:c.1171C>G , LRG_750t1:c.1171C>G
|
NP_109587.1:p.Gln391Glu
|
|
XM_006722799.2:c.892C>G
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XP_006722862.1:p.Gln298Glu
|
|
XM_011528133.1:c.601C>G
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XP_011526435.1:p.Gln201Glu
|
|
NM_030662.4:c.1171C>G
MANE Select
|
NP_109587.1:p.Gln391Glu
|
|