ENST00000394867.9:n.1544A>G
|
|
|
ENST00000688002.1:n.3256A>G
|
|
|
ENST00000688751.1:n.241A>G
|
|
|
ENST00000689792.1:n.1009A>G
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|
|
ENST00000262948.10:c.1105A>G
MANE Select
|
ENSP00000262948.4:p.Ile369Val
|
|
ENST00000262948.9:c.1105A>G
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ENSP00000262948.3:p.Ile369Val
|
|
ENST00000394867.8:c.814A>G
|
ENSP00000378336.1:p.Ile272Val
|
|
ENST00000597263.5:n.290A>G
|
|
|
ENST00000599021.1:c.215A>G
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|
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ENST00000600584.5:n.2554A>G
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|
|
ENST00000601786.5:n.1406A>G
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|
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NM_030662.3:c.1105A>G , LRG_750t1:c.1105A>G
|
NP_109587.1:p.Ile369Val
|
|
XM_006722799.2:c.826A>G
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XP_006722862.1:p.Ile276Val
|
|
XM_011528133.1:c.535A>G
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XP_011526435.1:p.Ile179Val
|
|
NM_030662.4:c.1105A>G
MANE Select
|
NP_109587.1:p.Ile369Val
|
|