ENST00000255078.8:c.2390C>T
MANE Select
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ENSP00000255078.4:p.Ala797Val
|
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ENST00000674675.1:c.587+47C>T
|
|
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ENST00000674878.1:c.548-53C>T
|
|
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ENST00000675118.1:c.1878C>T
|
|
|
ENST00000675389.1:n.665C>T
|
|
|
ENST00000675615.1:c.2390C>T
|
ENSP00000502413.1:p.Ala797Val
|
|
ENST00000675648.1:n.1765C>T
|
|
|
ENST00000675916.1:c.634C>T
|
|
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ENST00000676173.1:n.3135C>T
|
|
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ENST00000676182.1:c.821C>T
|
|
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ENST00000676228.1:c.*1713C>T
|
ENSP00000502375.1:n.*1713C>T
|
|
ENST00000255078.7:c.2390C>T
|
ENSP00000255078.3:p.Ala797Val
|
|
ENST00000539064.5:n.2149C>T
|
|
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ENST00000543739.5:n.1383C>T
|
|
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NM_002180.2:c.2390C>T , LRG_250t1:c.2390C>T
|
NP_002171.2:p.Ala797Val
|
|
XM_005273974.2:c.1379C>T
|
XP_005274031.1:p.Ala460Val
|
|
XM_005273975.2:c.1262C>T
|
XP_005274032.1:p.Ala421Val
|
|
XM_011544994.1:c.1157C>T
|
XP_011543296.1:p.Ala386Val
|
|
XR_949903.1:n.2492C>T
|
|
|
XM_005273975.3:c.1262C>T
|
XP_005274032.1:p.Ala421Val
|
|
XM_017017669.2:c.1379C>T
|
XP_016873158.1:p.Ala460Val
|
|
XM_017017670.2:c.1379C>T
|
XP_016873159.1:p.Ala460Val
|
|
XR_949903.3:n.2488C>T
|
|
|
NM_002180.3:c.2390C>T
MANE Select
|
NP_002171.2:p.Ala797Val
|
|