ENST00000255078.8:c.2178G>T
MANE Select
|
ENSP00000255078.4:p.Val726=
|
|
ENST00000674675.1:c.422G>T
|
|
|
ENST00000674878.1:c.422G>T
|
|
|
ENST00000674955.1:c.*895G>T
|
ENSP00000502463.1:n.*895G>T
|
|
ENST00000675118.1:c.1666G>T
|
|
|
ENST00000675389.1:n.453G>T
|
|
|
ENST00000675615.1:c.2178G>T
|
ENSP00000502413.1:p.Val726=
|
|
ENST00000675648.1:n.1553G>T
|
|
|
ENST00000675916.1:c.422G>T
|
|
|
ENST00000676173.1:n.2923G>T
|
|
|
ENST00000676182.1:c.609G>T
|
|
|
ENST00000676228.1:c.*1501G>T
|
ENSP00000502375.1:n.*1501G>T
|
|
ENST00000255078.7:c.2178G>T
|
ENSP00000255078.3:p.Val726=
|
|
ENST00000539064.5:n.1937G>T
|
|
|
ENST00000543739.5:n.1171G>T
|
|
|
NM_002180.2:c.2178G>T , LRG_250t1:c.2178G>T
|
NP_002171.2:p.Val726=
|
|
XM_005273974.2:c.1167G>T
|
XP_005274031.1:p.Val389=
|
|
XM_005273975.2:c.1050G>T
|
XP_005274032.1:p.Val350=
|
|
XM_011544994.1:c.945G>T
|
XP_011543296.1:p.Val315=
|
|
XR_949903.1:n.2280G>T
|
|
|
XM_005273975.3:c.1050G>T
|
XP_005274032.1:p.Val350=
|
|
XM_017017669.2:c.1167G>T
|
XP_016873158.1:p.Val389=
|
|
XM_017017670.2:c.1167G>T
|
XP_016873159.1:p.Val389=
|
|
XR_949903.3:n.2276G>T
|
|
|
NM_002180.3:c.2178G>T
MANE Select
|
NP_002171.2:p.Val726=
|
|