ENST00000394867.9:n.1583T=
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ENST00000688002.1:n.3295T=
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ENST00000688751.1:n.280T=
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ENST00000689792.1:n.1048T=
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ENST00000262948.10:c.1144T=
MANE Select
|
ENSP00000262948.4:p.Trp382=
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ENST00000262948.9:c.1144T=
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ENSP00000262948.3:p.Trp382=
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|
ENST00000394867.8:c.853T=
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ENSP00000378336.1:p.Trp285=
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ENST00000597263.5:n.329T=
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ENST00000599021.1:c.254T=
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|
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ENST00000600584.5:n.2593T=
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|
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ENST00000601786.5:n.1445T=
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|
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NM_030662.3:c.1144T= , LRG_750t1:c.1144T=
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NP_109587.1:p.Trp382=
|
|
XM_006722799.2:c.865T=
|
XP_006722862.1:p.Trp289=
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|
XM_011528133.1:c.574T=
|
XP_011526435.1:p.Trp192=
|
|
NM_030662.4:c.1144T=
MANE Select
|
NP_109587.1:p.Trp382=
|
|