ENST00000255078.8:c.1794C>T
MANE Select
|
ENSP00000255078.4:p.Asn598=
|
|
ENST00000674675.1:c.38C>T
|
|
|
ENST00000674878.1:c.38C>T
|
|
|
ENST00000674955.1:c.*511C>T
|
ENSP00000502463.1:n.*511C>T
|
|
ENST00000675118.1:c.1282C>T
|
|
|
ENST00000675389.1:n.69C>T
|
|
|
ENST00000675615.1:c.1794C>T
|
ENSP00000502413.1:p.Asn598=
|
|
ENST00000675648.1:n.1169C>T
|
|
|
ENST00000675916.1:c.38C>T
|
|
|
ENST00000676173.1:n.2539C>T
|
|
|
ENST00000676182.1:c.225C>T
|
|
|
ENST00000676228.1:c.*1117C>T
|
ENSP00000502375.1:n.*1117C>T
|
|
ENST00000255078.7:c.1794C>T
|
ENSP00000255078.3:p.Asn598=
|
|
ENST00000539064.5:n.1553C>T
|
|
|
ENST00000541229.5:n.489C>T
|
|
|
ENST00000543739.5:n.787C>T
|
|
|
ENST00000545475.1:n.390C>T
|
|
|
NM_002180.2:c.1794C>T , LRG_250t1:c.1794C>T
|
NP_002171.2:p.Asn598=
|
|
XM_005273974.2:c.783C>T
|
XP_005274031.1:p.Asn261=
|
|
XM_005273975.2:c.666C>T
|
XP_005274032.1:p.Asn222=
|
|
XM_011544994.1:c.561C>T
|
XP_011543296.1:p.Asn187=
|
|
XR_949903.1:n.1896C>T
|
|
|
XM_005273975.3:c.666C>T
|
XP_005274032.1:p.Asn222=
|
|
XM_017017669.2:c.783C>T
|
XP_016873158.1:p.Asn261=
|
|
XM_017017670.2:c.783C>T
|
XP_016873159.1:p.Asn261=
|
|
XR_949903.3:n.1892C>T
|
|
|
NM_002180.3:c.1794C>T
MANE Select
|
NP_002171.2:p.Asn598=
|
|