ENST00000394867.9:n.1606G=
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|
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ENST00000688002.1:n.3318G=
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|
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ENST00000688751.1:n.303G=
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|
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ENST00000689792.1:n.1071G=
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|
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ENST00000262948.10:c.1167G=
MANE Select
|
ENSP00000262948.4:p.Leu389=
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|
ENST00000262948.9:c.1167G=
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ENSP00000262948.3:p.Leu389=
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|
ENST00000394867.8:c.876G=
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ENSP00000378336.1:p.Leu292=
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|
ENST00000597263.5:n.352G=
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|
|
ENST00000599021.1:c.277G=
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|
|
ENST00000600584.5:n.2616G=
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|
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ENST00000601786.5:n.1468G=
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|
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NM_030662.3:c.1167G= , LRG_750t1:c.1167G=
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NP_109587.1:p.Leu389=
|
|
XM_006722799.2:c.888G=
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XP_006722862.1:p.Leu296=
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|
XM_011528133.1:c.597G=
|
XP_011526435.1:p.Leu199=
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|
NM_030662.4:c.1167G=
MANE Select
|
NP_109587.1:p.Leu389=
|
|