ENST00000255078.8:c.1416G>T
MANE Select
|
ENSP00000255078.4:p.Leu472=
|
|
ENST00000536803.2:n.327G>T
|
|
|
ENST00000674955.1:c.*133G>T
|
ENSP00000502463.1:n.*133G>T
|
|
ENST00000675118.1:c.904G>T
|
|
|
ENST00000675205.1:n.181G>T
|
|
|
ENST00000675310.1:n.553G>T
|
|
|
ENST00000675615.1:c.1416G>T
|
ENSP00000502413.1:p.Leu472=
|
|
ENST00000675648.1:n.791G>T
|
|
|
ENST00000675997.1:n.113-985G>T
|
|
|
ENST00000676149.1:n.490G>T
|
|
|
ENST00000676173.1:n.2161G>T
|
|
|
ENST00000676228.1:c.*739G>T
|
ENSP00000502375.1:n.*739G>T
|
|
ENST00000255078.7:c.1416G>T
|
ENSP00000255078.3:p.Leu472=
|
|
ENST00000537458.5:n.533G>T
|
|
|
ENST00000539064.5:n.1175G>T
|
|
|
ENST00000543739.5:n.533G>T
|
|
|
NM_002180.2:c.1416G>T , LRG_250t1:c.1416G>T
|
NP_002171.2:p.Leu472=
|
|
XM_005273974.2:c.405G>T
|
XP_005274031.1:p.Leu135=
|
|
XM_005273975.2:c.288G>T
|
XP_005274032.1:p.Leu96=
|
|
XM_011544994.1:c.183G>T
|
XP_011543296.1:p.Leu61=
|
|
XR_949903.1:n.1518G>T
|
|
|
XM_005273975.3:c.288G>T
|
XP_005274032.1:p.Leu96=
|
|
XM_017017669.2:c.405G>T
|
XP_016873158.1:p.Leu135=
|
|
XM_017017670.2:c.405G>T
|
XP_016873159.1:p.Leu135=
|
|
XM_017017671.2:c.1416G>T
|
XP_016873160.1:p.Leu472=
|
|
XR_949903.3:n.1514G>T
|
|
|
NM_002180.3:c.1416G>T
MANE Select
|
NP_002171.2:p.Leu472=
|
|