ENST00000330889.8:c.1012A>T
MANE Select
|
ENSP00000329468.3:p.Arg338Ter
|
|
ENST00000330889.7:c.1012A>T
|
ENSP00000329468.3:p.Arg338Ter
|
|
ENST00000470962.1:n.432A>T
|
|
|
ENST00000480980.1:n.446A>T
|
|
|
ENST00000580525.5:c.1030A>T
|
ENSP00000464121.1:p.Arg344Ter
|
|
ENST00000581285.5:c.928A>T
|
ENSP00000464155.1:p.Arg310Ter
|
|
ENST00000584828.5:c.381A>T
|
|
|
ENST00000585130.5:c.*611A>T
|
ENSP00000464120.1:n.*611A>T
|
|
NM_018404.2:c.1012A>T
|
NP_060874.1:p.Arg338Ter
|
|
XM_005258008.2:c.1030A>T
|
XP_005258065.1:p.Arg344Ter
|
|
XM_005258011.2:c.967A>T
|
XP_005258068.1:p.Arg323Ter
|
|
XM_006721973.2:c.1030A>T
|
XP_006722036.1:p.Arg344Ter
|
|
XM_011524993.1:c.1027A>T
|
XP_011523295.1:p.Arg343Ter
|
|
XM_011524994.1:c.1009A>T
|
XP_011523296.1:p.Arg337Ter
|
|
NM_001346712.1:c.1030A>T
|
NP_001333641.1:p.Arg344Ter
|
|
NM_001346714.1:c.1009A>T
|
NP_001333643.1:p.Arg337Ter
|
|
NM_001346716.1:c.1012A>T
|
NP_001333645.1:p.Arg338Ter
|
|
NR_144488.1:n.1211A>T
|
|
|
XM_024450831.1:c.1012A>T
|
XP_024306599.1:p.Arg338Ter
|
|
XM_024450832.1:c.1027A>T
|
XP_024306600.1:p.Arg343Ter
|
|
XM_024450833.1:c.967A>T
|
XP_024306601.1:p.Arg323Ter
|
|
XM_024450834.1:c.1030A>T
|
XP_024306602.1:p.Arg344Ter
|
|
XM_024450835.1:c.646A>T
|
XP_024306603.1:p.Arg216Ter
|
|
NM_018404.3:c.1012A>T
MANE Select
|
NP_060874.1:p.Arg338Ter
|
|
NM_001346712.2:c.1030A>T
|
NP_001333641.1:p.Arg344Ter
|
|
NM_001346714.2:c.1009A>T
|
NP_001333643.1:p.Arg337Ter
|
|
NM_001346716.2:c.1012A>T
|
NP_001333645.1:p.Arg338Ter
|
|
NR_144488.2:n.1002A>T
|
|
|