ENST00000255078.8:c.1419G>T
MANE Select
|
ENSP00000255078.4:p.Arg473Ser
|
|
ENST00000674955.1:c.*136G>T
|
ENSP00000502463.1:n.*136G>T
|
|
ENST00000675118.1:c.907G>T
|
|
|
ENST00000675205.1:n.183+314G>T
|
|
|
ENST00000675615.1:c.1419G>T
|
ENSP00000502413.1:p.Arg473Ser
|
|
ENST00000675648.1:n.794G>T
|
|
|
ENST00000675997.1:n.113-669G>T
|
|
|
ENST00000676173.1:n.2164G>T
|
|
|
ENST00000676228.1:c.*742G>T
|
ENSP00000502375.1:n.*742G>T
|
|
ENST00000255078.7:c.1419G>T
|
ENSP00000255078.3:p.Arg473Ser
|
|
ENST00000537458.5:n.536G>T
|
|
|
ENST00000539064.5:n.1178G>T
|
|
|
ENST00000541229.5:n.114G>T
|
|
|
ENST00000543739.5:n.536G>T
|
|
|
NM_002180.2:c.1419G>T , LRG_250t1:c.1419G>T
|
NP_002171.2:p.Arg473Ser
|
|
XM_005273974.2:c.408G>T
|
XP_005274031.1:p.Arg136Ser
|
|
XM_005273975.2:c.291G>T
|
XP_005274032.1:p.Arg97Ser
|
|
XM_011544994.1:c.186G>T
|
XP_011543296.1:p.Arg62Ser
|
|
XR_949903.1:n.1521G>T
|
|
|
XM_005273975.3:c.291G>T
|
XP_005274032.1:p.Arg97Ser
|
|
XM_017017669.2:c.408G>T
|
XP_016873158.1:p.Arg136Ser
|
|
XM_017017670.2:c.408G>T
|
XP_016873159.1:p.Arg136Ser
|
|
XM_017017671.2:c.1419G>T
|
XP_016873160.1:p.Arg473Ser
|
|
XR_949903.3:n.1517G>T
|
|
|
NM_002180.3:c.1419G>T
MANE Select
|
NP_002171.2:p.Arg473Ser
|
|