|
NM_203447.4:c.2464G>T
MANE Select
|
NP_982272.2:p.Glu822Ter
|
|
ENST00000432829.7:c.2464G>T
MANE Select
|
ENSP00000394888.3:p.Glu822Ter
|
|
NM_001190458.1:c.2260G>T
|
NP_001177387.1:p.Glu754Ter
|
|
NM_001190458.2:c.2260G>T
|
NP_001177387.1:p.Glu754Ter
|
|
NM_001193536.1:c.2260G>T
|
NP_001180465.1:p.Glu754Ter
|
|
NM_001193536.2:c.2260G>T
|
NP_001180465.1:p.Glu754Ter
|
|
NM_203447.3:c.2464G>T , LRG_196t1:c.2464G>T
|
NP_982272.2:p.Glu822Ter
|
|
ENST00000382329.1:c.865G>T
|
ENSP00000371766.1:p.Glu289Ter
|
|
ENST00000382329.2:c.2260G>T
|
ENSP00000371766.2:p.Glu754Ter
|
|
ENST00000382331.5:c.370G>T
|
ENSP00000371768.1:p.Glu124Ter
|
|
ENST00000382331.6:n.961G>T
|
|
|
ENST00000432829.6:c.2464G>T
|
ENSP00000394888.3:p.Glu822Ter
|
|
ENST00000453981.5:c.2260G>T
|
ENSP00000408464.2:p.Glu754Ter
|
|
ENST00000469391.5:c.2260G>T
|
ENSP00000419438.1:p.Glu754Ter
|
|
ENST00000483757.5:c.*1939G>T
|
ENSP00000417691.1:n.*1939G>T
|
|
ENST00000483757.6:c.*1151G>T
|
ENSP00000417691.2:n.*1151G>T
|
|
ENST00000495184.5:n.4419G>T
|
|
|
ENST00000682260.1:n.2360G>T
|
|
|
ENST00000685949.1:n.1252G>T
|
|
|
XM_011518045.1:c.2260G>T
|
XP_011516347.1:p.Glu754Ter
|
|
XM_011518045.3:c.2260G>T
|
XP_011516347.1:p.Glu754Ter
|
|
XM_011518046.1:c.2326G>T
|
XP_011516348.1:p.Glu776Ter
|
|
XM_011518046.2:c.2326G>T
|
XP_011516348.1:p.Glu776Ter
|
|
XM_011518047.1:c.2260G>T
|
XP_011516349.1:p.Glu754Ter
|
|
XM_011518047.3:c.2260G>T
|
XP_011516349.1:p.Glu754Ter
|
|
XM_011518048.1:c.2260G>T
|
XP_011516350.1:p.Glu754Ter
|
|
XM_011518048.2:c.2260G>T
|
XP_011516350.1:p.Glu754Ter
|
|
XM_011518049.1:c.700G>T
|
XP_011516351.1:p.Glu234Ter
|
|
XM_011518049.2:c.700G>T
|
XP_011516351.1:p.Glu234Ter
|
|
XM_017015173.1:c.2260G>T
|
XP_016870662.1:p.Glu754Ter
|
|
XM_017015174.1:c.2326G>T
|
XP_016870663.1:p.Glu776Ter
|