ENST00000394867.9:n.1636C>A
|
|
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ENST00000688002.1:n.3348C>A
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|
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ENST00000688751.1:n.333C>A
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|
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ENST00000689792.1:n.1101C>A
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|
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ENST00000262948.10:c.1197C>A
MANE Select
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ENSP00000262948.4:p.Ala399=
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ENST00000262948.9:c.1197C>A
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ENSP00000262948.3:p.Ala399=
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ENST00000394867.8:c.906C>A
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ENSP00000378336.1:p.Ala302=
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|
ENST00000597263.5:n.382C>A
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|
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ENST00000599021.1:c.307C>A
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ENST00000600584.5:n.2646C>A
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|
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ENST00000601786.5:n.1498C>A
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NM_030662.3:c.1197C>A , LRG_750t1:c.1197C>A
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NP_109587.1:p.Ala399=
|
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XM_006722799.2:c.918C>A
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XP_006722862.1:p.Ala306=
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XM_011528133.1:c.627C>A
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XP_011526435.1:p.Ala209=
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NM_030662.4:c.1197C>A
MANE Select
|
NP_109587.1:p.Ala399=
|
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