ENST00000407991.3:c.1258G>T
MANE Select
|
ENSP00000385026.1:p.Glu420Ter
|
|
ENST00000240132.7:c.1213G>T
|
ENSP00000240132.2:p.Glu405Ter
|
|
ENST00000407991.2:c.1258G>T
|
ENSP00000385026.1:p.Glu420Ter
|
|
ENST00000520600.1:n.290-1431G>T
|
|
|
ENST00000520933.7:c.1192G>T
|
ENSP00000429616.2:p.Glu398Ter
|
|
ENST00000523695.5:c.*660G>T
|
ENSP00000430612.1:n.*660G>T
|
|
NM_000742.3:c.1258G>T
|
NP_000733.2:p.Glu420Ter
|
|
NM_001282455.1:c.1213G>T
|
NP_001269384.1:p.Glu405Ter
|
|
XM_005273397.1:c.781G>T
|
XP_005273454.1:p.Glu261Ter
|
|
XM_006716282.1:c.1258G>T
|
XP_006716345.1:p.Glu420Ter
|
|
XM_011544388.1:c.1258G>T
|
XP_011542690.1:p.Glu420Ter
|
|
XM_011544389.1:c.664G>T
|
XP_011542691.1:p.Glu222Ter
|
|
NM_001347705.1:c.781G>T
|
NP_001334634.1:p.Glu261Ter
|
|
NM_001347706.1:c.781G>T
|
NP_001334635.1:p.Glu261Ter
|
|
NM_001347707.1:c.664G>T
|
NP_001334636.1:p.Glu222Ter
|
|
NM_001347708.1:c.664G>T
|
NP_001334637.1:p.Glu222Ter
|
|
XM_011544389.2:c.664G>T
|
XP_011542691.1:p.Glu222Ter
|
|
NM_000742.4:c.1258G>T
MANE Select
|
NP_000733.2:p.Glu420Ter
|
|
NM_001282455.2:c.1213G>T
|
NP_001269384.1:p.Glu405Ter
|
|
NM_001347705.2:c.781G>T
|
NP_001334634.1:p.Glu261Ter
|
|
NM_001347706.2:c.781G>T
|
NP_001334635.1:p.Glu261Ter
|
|
NM_001347707.2:c.664G>T
|
NP_001334636.1:p.Glu222Ter
|
|
NM_001347708.2:c.664G>T
|
NP_001334637.1:p.Glu222Ter
|
|