ENST00000255078.8:c.2922T>A
MANE Select
|
ENSP00000255078.4:p.Asp974Glu
|
|
ENST00000675118.1:c.2410T>A
|
|
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ENST00000675615.1:c.*121T>A
|
ENSP00000502413.1:n.*121T>A
|
|
ENST00000675648.1:n.2484T>A
|
|
|
ENST00000675916.1:c.1353T>A
|
|
|
ENST00000676173.1:n.3667T>A
|
|
|
ENST00000255078.7:c.2922T>A
|
ENSP00000255078.3:p.Asp974Glu
|
|
ENST00000543739.5:n.1915T>A
|
|
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ENST00000544521.1:n.753T>A
|
|
|
NM_002180.2:c.2922T>A , LRG_250t1:c.2922T>A
|
NP_002171.2:p.Asp974Glu
|
|
XM_005273974.2:c.1911T>A
|
XP_005274031.1:p.Asp637Glu
|
|
XM_005273975.2:c.1794T>A
|
XP_005274032.1:p.Asp598Glu
|
|
XM_011544994.1:c.1689T>A
|
XP_011543296.1:p.Asp563Glu
|
|
XR_949903.1:n.3211T>A
|
|
|
XM_005273975.3:c.1794T>A
|
XP_005274032.1:p.Asp598Glu
|
|
XM_017017669.2:c.1911T>A
|
XP_016873158.1:p.Asp637Glu
|
|
XM_017017670.2:c.1911T>A
|
XP_016873159.1:p.Asp637Glu
|
|
XR_949903.3:n.3207T>A
|
|
|
NM_002180.3:c.2922T>A
MANE Select
|
NP_002171.2:p.Asp974Glu
|
|