ENST00000255078.8:c.2449C>A
MANE Select
|
ENSP00000255078.4:p.Gln817Lys
|
|
ENST00000674675.1:c.594C>A
|
|
|
ENST00000674878.1:c.554C>A
|
|
|
ENST00000675118.1:c.1937C>A
|
|
|
ENST00000675389.1:n.724C>A
|
|
|
ENST00000675615.1:c.2449C>A
|
ENSP00000502413.1:p.Gln817Lys
|
|
ENST00000675648.1:n.1824C>A
|
|
|
ENST00000675916.1:c.693C>A
|
|
|
ENST00000676173.1:n.3194C>A
|
|
|
ENST00000676182.1:c.880C>A
|
|
|
ENST00000676228.1:c.*1772C>A
|
ENSP00000502375.1:n.*1772C>A
|
|
ENST00000255078.7:c.2449C>A
|
ENSP00000255078.3:p.Gln817Lys
|
|
ENST00000539064.5:n.2208C>A
|
|
|
ENST00000543739.5:n.1442C>A
|
|
|
NM_002180.2:c.2449C>A , LRG_250t1:c.2449C>A
|
NP_002171.2:p.Gln817Lys
|
|
XM_005273974.2:c.1438C>A
|
XP_005274031.1:p.Gln480Lys
|
|
XM_005273975.2:c.1321C>A
|
XP_005274032.1:p.Gln441Lys
|
|
XM_011544994.1:c.1216C>A
|
XP_011543296.1:p.Gln406Lys
|
|
XR_949903.1:n.2551C>A
|
|
|
XM_005273975.3:c.1321C>A
|
XP_005274032.1:p.Gln441Lys
|
|
XM_017017669.2:c.1438C>A
|
XP_016873158.1:p.Gln480Lys
|
|
XM_017017670.2:c.1438C>A
|
XP_016873159.1:p.Gln480Lys
|
|
XR_949903.3:n.2547C>A
|
|
|
NM_002180.3:c.2449C>A
MANE Select
|
NP_002171.2:p.Gln817Lys
|
|