ENST00000394867.9:n.1438G=
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|
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ENST00000688002.1:n.3150G=
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|
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ENST00000688751.1:n.135G=
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|
|
ENST00000689792.1:n.903G=
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|
|
ENST00000262948.10:c.999G=
MANE Select
|
ENSP00000262948.4:p.Leu333=
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|
ENST00000262948.9:c.999G=
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ENSP00000262948.3:p.Leu333=
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|
ENST00000394867.8:c.708G=
|
ENSP00000378336.1:p.Leu236=
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ENST00000595715.1:n.814G=
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|
|
ENST00000597263.5:n.184G=
|
|
|
ENST00000599021.1:c.109G=
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|
|
ENST00000600584.5:n.1559G=
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|
|
ENST00000601786.5:n.1300G=
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|
|
NM_030662.3:c.999G= , LRG_750t1:c.999G=
|
NP_109587.1:p.Leu333=
|
|
XM_006722799.2:c.720G=
|
XP_006722862.1:p.Leu240=
|
|
XM_011528133.1:c.429G=
|
XP_011526435.1:p.Leu143=
|
|
XM_017026989.1:c.999G=
|
XP_016882478.1:p.Leu333=
|
|
XM_017026990.1:c.720G=
|
XP_016882479.1:p.Leu240=
|
|
NM_030662.4:c.999G=
MANE Select
|
NP_109587.1:p.Leu333=
|
|