ENST00000394867.9:n.1446G>T
|
|
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ENST00000688002.1:n.3158G>T
|
|
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ENST00000688751.1:n.143G>T
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|
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ENST00000689792.1:n.911G>T
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|
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ENST00000262948.10:c.1007G>T
MANE Select
|
ENSP00000262948.4:p.Gly336Val
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ENST00000262948.9:c.1007G>T
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ENSP00000262948.3:p.Gly336Val
|
|
ENST00000394867.8:c.716G>T
|
ENSP00000378336.1:p.Gly239Val
|
|
ENST00000595715.1:n.822G>T
|
|
|
ENST00000597263.5:n.192G>T
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|
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ENST00000599021.1:c.117G>T
|
|
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ENST00000600584.5:n.1567G>T
|
|
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ENST00000601786.5:n.1308G>T
|
|
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NM_030662.3:c.1007G>T , LRG_750t1:c.1007G>T
|
NP_109587.1:p.Gly336Val
|
|
XM_006722799.2:c.728G>T
|
XP_006722862.1:p.Gly243Val
|
|
XM_011528133.1:c.437G>T
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XP_011526435.1:p.Gly146Val
|
|
XM_017026989.1:c.1007G>T
|
XP_016882478.1:p.Gly336Val
|
|
XM_017026990.1:c.728G>T
|
XP_016882479.1:p.Gly243Val
|
|
NM_030662.4:c.1007G>T
MANE Select
|
NP_109587.1:p.Gly336Val
|
|