ENST00000435881.7:c.688G=
MANE Select
|
ENSP00000416627.1:p.Glu230=
|
|
ENST00000246912.8:c.850G=
|
ENSP00000246912.3:p.Glu284=
|
|
ENST00000346833.8:c.598G=
|
ENSP00000320913.3:p.Glu200=
|
|
ENST00000435881.6:c.688G=
|
ENSP00000416627.1:p.Glu230=
|
|
ENST00000585403.5:n.895G=
|
|
|
ENST00000588320.1:n.1164G=
|
|
|
ENST00000590050.5:n.854G=
|
|
|
NM_170607.2:c.850G=
|
NP_733752.1:p.Glu284=
|
|
NM_198204.1:c.688G=
|
NP_937847.1:p.Glu230=
|
|
NM_198205.1:c.598G=
|
NP_937848.1:p.Glu200=
|
|
NM_198204.2:c.688G=
MANE Select
|
NP_937847.1:p.Glu230=
|
|
NM_170607.3:c.850G=
|
NP_733752.1:p.Glu284=
|
|
NM_198205.2:c.598G=
|
NP_937848.1:p.Glu200=
|
|