ENST00000255078.8:c.2441A>G
MANE Select
|
ENSP00000255078.4:p.Gln814Arg
|
|
ENST00000674675.1:c.588-2A>G
|
|
|
ENST00000674878.1:c.548-2A>G
|
|
|
ENST00000675118.1:c.1929A>G
|
|
|
ENST00000675389.1:n.716A>G
|
|
|
ENST00000675615.1:c.2441A>G
|
ENSP00000502413.1:p.Gln814Arg
|
|
ENST00000675648.1:n.1816A>G
|
|
|
ENST00000675916.1:c.685A>G
|
|
|
ENST00000676173.1:n.3186A>G
|
|
|
ENST00000676182.1:c.872A>G
|
|
|
ENST00000676228.1:c.*1764A>G
|
ENSP00000502375.1:n.*1764A>G
|
|
ENST00000255078.7:c.2441A>G
|
ENSP00000255078.3:p.Gln814Arg
|
|
ENST00000539064.5:n.2200A>G
|
|
|
ENST00000543739.5:n.1434A>G
|
|
|
NM_002180.2:c.2441A>G , LRG_250t1:c.2441A>G
|
NP_002171.2:p.Gln814Arg
|
|
XM_005273974.2:c.1430A>G
|
XP_005274031.1:p.Gln477Arg
|
|
XM_005273975.2:c.1313A>G
|
XP_005274032.1:p.Gln438Arg
|
|
XM_011544994.1:c.1208A>G
|
XP_011543296.1:p.Gln403Arg
|
|
XR_949903.1:n.2543A>G
|
|
|
XM_005273975.3:c.1313A>G
|
XP_005274032.1:p.Gln438Arg
|
|
XM_017017669.2:c.1430A>G
|
XP_016873158.1:p.Gln477Arg
|
|
XM_017017670.2:c.1430A>G
|
XP_016873159.1:p.Gln477Arg
|
|
XR_949903.3:n.2539A>G
|
|
|
NM_002180.3:c.2441A>G
MANE Select
|
NP_002171.2:p.Gln814Arg
|
|