ENST00000398603.6:c.364G=
|
ENSP00000381604.1:p.Asp122=
|
|
ENST00000398606.10:c.472G=
MANE Select
|
ENSP00000381607.3:p.Asp158=
|
|
ENST00000646888.1:c.*188G=
|
ENSP00000494477.1:n.*188G=
|
|
ENST00000398603.5:c.364G=
|
ENSP00000381604.1:p.Asp122=
|
|
ENST00000398606.7:c.472G=
|
ENSP00000381607.3:p.Asp158=
|
|
ENST00000467591.1:n.583G=
|
|
|
ENST00000494593.1:n.1444G=
|
|
|
ENST00000495996.1:c.198G=
|
ENSP00000484686.1:p.Trp66=
|
|
ENST00000498765.5:c.535G=
|
|
|
NM_000852.3:c.472G= , LRG_723t1:c.472G=
|
NP_000843.1:p.Asp158=
|
|
NM_000852.4:c.472G=
MANE Select
|
NP_000843.1:p.Asp158=
|
|