ENST00000255078.8:c.1782C>A
MANE Select
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ENSP00000255078.4:p.Asp594Glu
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ENST00000674675.1:c.26C>A
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ENST00000674878.1:c.26C>A
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ENST00000674955.1:c.*499C>A
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ENSP00000502463.1:n.*499C>A
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ENST00000675118.1:c.1270C>A
|
|
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ENST00000675389.1:n.57C>A
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|
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ENST00000675615.1:c.1782C>A
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ENSP00000502413.1:p.Asp594Glu
|
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ENST00000675648.1:n.1157C>A
|
|
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ENST00000675916.1:c.26C>A
|
|
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ENST00000676173.1:n.2527C>A
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ENST00000676182.1:c.213C>A
|
|
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ENST00000676228.1:c.*1105C>A
|
ENSP00000502375.1:n.*1105C>A
|
|
ENST00000255078.7:c.1782C>A
|
ENSP00000255078.3:p.Asp594Glu
|
|
ENST00000539064.5:n.1541C>A
|
|
|
ENST00000541229.5:n.477C>A
|
|
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ENST00000543739.5:n.775C>A
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|
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ENST00000545475.1:n.378C>A
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|
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NM_002180.2:c.1782C>A , LRG_250t1:c.1782C>A
|
NP_002171.2:p.Asp594Glu
|
|
XM_005273974.2:c.771C>A
|
XP_005274031.1:p.Asp257Glu
|
|
XM_005273975.2:c.654C>A
|
XP_005274032.1:p.Asp218Glu
|
|
XM_011544994.1:c.549C>A
|
XP_011543296.1:p.Asp183Glu
|
|
XR_949903.1:n.1884C>A
|
|
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XM_005273975.3:c.654C>A
|
XP_005274032.1:p.Asp218Glu
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XM_017017669.2:c.771C>A
|
XP_016873158.1:p.Asp257Glu
|
|
XM_017017670.2:c.771C>A
|
XP_016873159.1:p.Asp257Glu
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|
XR_949903.3:n.1880C>A
|
|
|
NM_002180.3:c.1782C>A
MANE Select
|
NP_002171.2:p.Asp594Glu
|
|