ENST00000255078.8:c.2290G>T
MANE Select
|
ENSP00000255078.4:p.Glu764Ter
|
|
ENST00000674675.1:c.534G>T
|
|
|
ENST00000674878.1:c.534G>T
|
|
|
ENST00000674955.1:c.*1007G>T
|
ENSP00000502463.1:n.*1007G>T
|
|
ENST00000675118.1:c.1778G>T
|
|
|
ENST00000675389.1:n.565G>T
|
|
|
ENST00000675615.1:c.2290G>T
|
ENSP00000502413.1:p.Glu764Ter
|
|
ENST00000675648.1:n.1665G>T
|
|
|
ENST00000675916.1:c.534G>T
|
|
|
ENST00000676173.1:n.3035G>T
|
|
|
ENST00000676182.1:c.721G>T
|
|
|
ENST00000676228.1:c.*1613G>T
|
ENSP00000502375.1:n.*1613G>T
|
|
ENST00000255078.7:c.2290G>T
|
ENSP00000255078.3:p.Glu764Ter
|
|
ENST00000539064.5:n.2049G>T
|
|
|
ENST00000543739.5:n.1283G>T
|
|
|
NM_002180.2:c.2290G>T , LRG_250t1:c.2290G>T
|
NP_002171.2:p.Glu764Ter
|
|
XM_005273974.2:c.1279G>T
|
XP_005274031.1:p.Glu427Ter
|
|
XM_005273975.2:c.1162G>T
|
XP_005274032.1:p.Glu388Ter
|
|
XM_011544994.1:c.1057G>T
|
XP_011543296.1:p.Glu353Ter
|
|
XR_949903.1:n.2392G>T
|
|
|
XM_005273975.3:c.1162G>T
|
XP_005274032.1:p.Glu388Ter
|
|
XM_017017669.2:c.1279G>T
|
XP_016873158.1:p.Glu427Ter
|
|
XM_017017670.2:c.1279G>T
|
XP_016873159.1:p.Glu427Ter
|
|
XR_949903.3:n.2388G>T
|
|
|
NM_002180.3:c.2290G>T
MANE Select
|
NP_002171.2:p.Glu764Ter
|
|