ENST00000394867.9:n.1585G=
|
|
|
ENST00000688002.1:n.3297G=
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|
|
ENST00000688751.1:n.282G=
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|
|
ENST00000689792.1:n.1050G=
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|
|
ENST00000262948.10:c.1146G=
MANE Select
|
ENSP00000262948.4:p.Trp382=
|
|
ENST00000262948.9:c.1146G=
|
ENSP00000262948.3:p.Trp382=
|
|
ENST00000394867.8:c.855G=
|
ENSP00000378336.1:p.Trp285=
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|
ENST00000597263.5:n.331G=
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|
|
ENST00000599021.1:c.256G=
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|
|
ENST00000600584.5:n.2595G=
|
|
|
ENST00000601786.5:n.1447G=
|
|
|
NM_030662.3:c.1146G= , LRG_750t1:c.1146G=
|
NP_109587.1:p.Trp382=
|
|
XM_006722799.2:c.867G=
|
XP_006722862.1:p.Trp289=
|
|
XM_011528133.1:c.576G=
|
XP_011526435.1:p.Trp192=
|
|
NM_030662.4:c.1146G=
MANE Select
|
NP_109587.1:p.Trp382=
|
|