ENST00000394867.9:n.1612G>A
|
|
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ENST00000688002.1:n.3324G>A
|
|
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ENST00000688751.1:n.309G>A
|
|
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ENST00000689792.1:n.1077G>A
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|
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ENST00000262948.10:c.1173G>A
MANE Select
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ENSP00000262948.4:p.Gln391=
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|
ENST00000262948.9:c.1173G>A
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ENSP00000262948.3:p.Gln391=
|
|
ENST00000394867.8:c.882G>A
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ENSP00000378336.1:p.Gln294=
|
|
ENST00000597263.5:n.358G>A
|
|
|
ENST00000599021.1:c.283G>A
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|
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ENST00000600584.5:n.2622G>A
|
|
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ENST00000601786.5:n.1474G>A
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|
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NM_030662.3:c.1173G>A , LRG_750t1:c.1173G>A
|
NP_109587.1:p.Gln391=
|
|
XM_006722799.2:c.894G>A
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XP_006722862.1:p.Gln298=
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|
XM_011528133.1:c.603G>A
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XP_011526435.1:p.Gln201=
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|
NM_030662.4:c.1173G>A
MANE Select
|
NP_109587.1:p.Gln391=
|
|