ENST00000394867.9:n.1616G>A
|
|
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ENST00000688002.1:n.3328G>A
|
|
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ENST00000688751.1:n.313G>A
|
|
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ENST00000689792.1:n.1081G>A
|
|
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ENST00000262948.10:c.1177G>A
MANE Select
|
ENSP00000262948.4:p.Gly393Ser
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|
ENST00000262948.9:c.1177G>A
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ENSP00000262948.3:p.Gly393Ser
|
|
ENST00000394867.8:c.886G>A
|
ENSP00000378336.1:p.Gly296Ser
|
|
ENST00000597263.5:n.362G>A
|
|
|
ENST00000599021.1:c.287G>A
|
|
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ENST00000600584.5:n.2626G>A
|
|
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ENST00000601786.5:n.1478G>A
|
|
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NM_030662.3:c.1177G>A , LRG_750t1:c.1177G>A
|
NP_109587.1:p.Gly393Ser
|
|
XM_006722799.2:c.898G>A
|
XP_006722862.1:p.Gly300Ser
|
|
XM_011528133.1:c.607G>A
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XP_011526435.1:p.Gly203Ser
|
|
NM_030662.4:c.1177G>A
MANE Select
|
NP_109587.1:p.Gly393Ser
|
|