ENST00000255078.8:c.2439G>T
MANE Select
|
ENSP00000255078.4:p.Ala813=
|
|
ENST00000674675.1:c.588-4G>T
|
|
|
ENST00000674878.1:c.548-4G>T
|
|
|
ENST00000675118.1:c.1927G>T
|
|
|
ENST00000675389.1:n.714G>T
|
|
|
ENST00000675615.1:c.2439G>T
|
ENSP00000502413.1:p.Ala813=
|
|
ENST00000675648.1:n.1814G>T
|
|
|
ENST00000675916.1:c.683G>T
|
|
|
ENST00000676173.1:n.3184G>T
|
|
|
ENST00000676182.1:c.870G>T
|
|
|
ENST00000676228.1:c.*1762G>T
|
ENSP00000502375.1:n.*1762G>T
|
|
ENST00000255078.7:c.2439G>T
|
ENSP00000255078.3:p.Ala813=
|
|
ENST00000539064.5:n.2198G>T
|
|
|
ENST00000543739.5:n.1432G>T
|
|
|
NM_002180.2:c.2439G>T , LRG_250t1:c.2439G>T
|
NP_002171.2:p.Ala813=
|
|
XM_005273974.2:c.1428G>T
|
XP_005274031.1:p.Ala476=
|
|
XM_005273975.2:c.1311G>T
|
XP_005274032.1:p.Ala437=
|
|
XM_011544994.1:c.1206G>T
|
XP_011543296.1:p.Ala402=
|
|
XR_949903.1:n.2541G>T
|
|
|
XM_005273975.3:c.1311G>T
|
XP_005274032.1:p.Ala437=
|
|
XM_017017669.2:c.1428G>T
|
XP_016873158.1:p.Ala476=
|
|
XM_017017670.2:c.1428G>T
|
XP_016873159.1:p.Ala476=
|
|
XR_949903.3:n.2537G>T
|
|
|
NM_002180.3:c.2439G>T
MANE Select
|
NP_002171.2:p.Ala813=
|
|