ENST00000255078.8:c.1792A>G
MANE Select
|
ENSP00000255078.4:p.Asn598Asp
|
|
ENST00000674675.1:c.36A>G
|
|
|
ENST00000674878.1:c.36A>G
|
|
|
ENST00000674955.1:c.*509A>G
|
ENSP00000502463.1:n.*509A>G
|
|
ENST00000675118.1:c.1280A>G
|
|
|
ENST00000675389.1:n.67A>G
|
|
|
ENST00000675615.1:c.1792A>G
|
ENSP00000502413.1:p.Asn598Asp
|
|
ENST00000675648.1:n.1167A>G
|
|
|
ENST00000675916.1:c.36A>G
|
|
|
ENST00000676173.1:n.2537A>G
|
|
|
ENST00000676182.1:c.223A>G
|
|
|
ENST00000676228.1:c.*1115A>G
|
ENSP00000502375.1:n.*1115A>G
|
|
ENST00000255078.7:c.1792A>G
|
ENSP00000255078.3:p.Asn598Asp
|
|
ENST00000539064.5:n.1551A>G
|
|
|
ENST00000541229.5:n.487A>G
|
|
|
ENST00000543739.5:n.785A>G
|
|
|
ENST00000545475.1:n.388A>G
|
|
|
NM_002180.2:c.1792A>G , LRG_250t1:c.1792A>G
|
NP_002171.2:p.Asn598Asp
|
|
XM_005273974.2:c.781A>G
|
XP_005274031.1:p.Asn261Asp
|
|
XM_005273975.2:c.664A>G
|
XP_005274032.1:p.Asn222Asp
|
|
XM_011544994.1:c.559A>G
|
XP_011543296.1:p.Asn187Asp
|
|
XR_949903.1:n.1894A>G
|
|
|
XM_005273975.3:c.664A>G
|
XP_005274032.1:p.Asn222Asp
|
|
XM_017017669.2:c.781A>G
|
XP_016873158.1:p.Asn261Asp
|
|
XM_017017670.2:c.781A>G
|
XP_016873159.1:p.Asn261Asp
|
|
XR_949903.3:n.1890A>G
|
|
|
NM_002180.3:c.1792A>G
MANE Select
|
NP_002171.2:p.Asn598Asp
|
|