ENST00000330062.8:c.678G=
MANE Select
|
ENSP00000331897.4:p.Glu226=
|
|
ENST00000330062.7:c.678G=
|
ENSP00000331897.3:p.Glu226=
|
|
ENST00000540499.2:c.522G=
|
ENSP00000446147.2:p.Glu174=
|
|
ENST00000559482.5:c.351G=
|
ENSP00000453016.1:p.Glu117=
|
|
ENST00000560061.1:c.*303G=
|
ENSP00000453254.1:n.*303G=
|
|
NM_001289910.1:c.522G= , LRG_611t1:c.522G=
|
NP_001276839.1:p.Glu174=
|
|
NM_001290114.1:c.288G=
|
NP_001277043.1:p.Glu96=
|
|
NM_002168.3:c.678G= , LRG_611t2:c.678G=
|
NP_002159.2:p.Glu226=
|
|
NM_001290114.2:c.288G=
|
NP_001277043.1:p.Glu96=
|
|
NM_002168.4:c.678G=
MANE Select
|
NP_002159.2:p.Glu226=
|
|