ENST00000255078.8:c.2201T>A
MANE Select
|
ENSP00000255078.4:p.Val734Glu
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ENST00000674675.1:c.445T>A
|
|
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ENST00000674878.1:c.445T>A
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|
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ENST00000674955.1:c.*918T>A
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ENSP00000502463.1:n.*918T>A
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ENST00000675118.1:c.1689T>A
|
|
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ENST00000675389.1:n.476T>A
|
|
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ENST00000675615.1:c.2201T>A
|
ENSP00000502413.1:p.Val734Glu
|
|
ENST00000675648.1:n.1576T>A
|
|
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ENST00000675916.1:c.445T>A
|
|
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ENST00000676173.1:n.2946T>A
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|
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ENST00000676182.1:c.632T>A
|
|
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ENST00000676228.1:c.*1524T>A
|
ENSP00000502375.1:n.*1524T>A
|
|
ENST00000255078.7:c.2201T>A
|
ENSP00000255078.3:p.Val734Glu
|
|
ENST00000539064.5:n.1960T>A
|
|
|
ENST00000543739.5:n.1194T>A
|
|
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NM_002180.2:c.2201T>A , LRG_250t1:c.2201T>A
|
NP_002171.2:p.Val734Glu
|
|
XM_005273974.2:c.1190T>A
|
XP_005274031.1:p.Val397Glu
|
|
XM_005273975.2:c.1073T>A
|
XP_005274032.1:p.Val358Glu
|
|
XM_011544994.1:c.968T>A
|
XP_011543296.1:p.Val323Glu
|
|
XR_949903.1:n.2303T>A
|
|
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XM_005273975.3:c.1073T>A
|
XP_005274032.1:p.Val358Glu
|
|
XM_017017669.2:c.1190T>A
|
XP_016873158.1:p.Val397Glu
|
|
XM_017017670.2:c.1190T>A
|
XP_016873159.1:p.Val397Glu
|
|
XR_949903.3:n.2299T>A
|
|
|
NM_002180.3:c.2201T>A
MANE Select
|
NP_002171.2:p.Val734Glu
|
|