ENST00000553591.2:c.216T>G
|
ENSP00000452421.2:p.Ser72=
|
|
ENST00000556293.6:n.218T>G
|
|
|
ENST00000556754.2:n.1161T>G
|
|
|
ENST00000557229.6:n.218T>G
|
|
|
ENST00000697613.1:c.99T>G
|
ENSP00000513359.1:p.Ser33=
|
|
ENST00000697614.1:c.-139T>G
|
ENSP00000513360.1:n.-139T>G
|
|
ENST00000697615.1:n.617T>G
|
|
|
ENST00000361505.10:c.99T>G
MANE Select
|
ENSP00000354532.6:p.Ser33=
|
|
ENST00000361505.9:c.99T>G
|
ENSP00000354532.5:p.Ser33=
|
|
ENST00000553418.5:c.99T>G
|
ENSP00000450663.1:p.Ser33=
|
|
ENST00000553591.1:c.216T>G
|
ENSP00000452421.1:p.Ser72=
|
|
ENST00000554056.5:n.210T>G
|
|
|
ENST00000554065.1:c.-139T>G
|
ENSP00000451108.1:n.-139T>G
|
|
ENST00000556293.5:n.218T>G
|
|
|
ENST00000557229.5:n.218T>G
|
|
|
NM_000270.3:c.99T>G , LRG_91t1:c.99T>G
|
NP_000261.2:p.Ser33=
|
|
NM_000270.4:c.99T>G
MANE Select
|
NP_000261.2:p.Ser33=
|
|