ENST00000255078.8:c.2262C>A
MANE Select
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ENSP00000255078.4:p.Asp754Glu
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ENST00000674675.1:c.506C>A
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ENST00000674878.1:c.506C>A
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ENST00000674955.1:c.*979C>A
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ENSP00000502463.1:n.*979C>A
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ENST00000675118.1:c.1750C>A
|
|
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ENST00000675389.1:n.537C>A
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|
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ENST00000675615.1:c.2262C>A
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ENSP00000502413.1:p.Asp754Glu
|
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ENST00000675648.1:n.1637C>A
|
|
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ENST00000675916.1:c.506C>A
|
|
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ENST00000676173.1:n.3007C>A
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ENST00000676182.1:c.693C>A
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|
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ENST00000676228.1:c.*1585C>A
|
ENSP00000502375.1:n.*1585C>A
|
|
ENST00000255078.7:c.2262C>A
|
ENSP00000255078.3:p.Asp754Glu
|
|
ENST00000539064.5:n.2021C>A
|
|
|
ENST00000543739.5:n.1255C>A
|
|
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NM_002180.2:c.2262C>A , LRG_250t1:c.2262C>A
|
NP_002171.2:p.Asp754Glu
|
|
XM_005273974.2:c.1251C>A
|
XP_005274031.1:p.Asp417Glu
|
|
XM_005273975.2:c.1134C>A
|
XP_005274032.1:p.Asp378Glu
|
|
XM_011544994.1:c.1029C>A
|
XP_011543296.1:p.Asp343Glu
|
|
XR_949903.1:n.2364C>A
|
|
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XM_005273975.3:c.1134C>A
|
XP_005274032.1:p.Asp378Glu
|
|
XM_017017669.2:c.1251C>A
|
XP_016873158.1:p.Asp417Glu
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XM_017017670.2:c.1251C>A
|
XP_016873159.1:p.Asp417Glu
|
|
XR_949903.3:n.2360C>A
|
|
|
NM_002180.3:c.2262C>A
MANE Select
|
NP_002171.2:p.Asp754Glu
|
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