ENST00000398603.6:c.337-206G=
|
ENSP00000381604.1:n.337-206G=
|
|
ENST00000398606.10:c.416G=
MANE Select
|
ENSP00000381607.3:p.Gly139=
|
|
ENST00000646888.1:c.*132G=
|
ENSP00000494477.1:n.*132G=
|
|
ENST00000398603.5:c.337-206G=
|
ENSP00000381604.1:n.337-206G=
|
|
ENST00000398606.7:c.416G=
|
ENSP00000381607.3:p.Gly139=
|
|
ENST00000467591.1:n.527G=
|
|
|
ENST00000494593.1:n.1211G=
|
|
|
ENST00000495996.1:c.80G=
|
ENSP00000484686.1:p.Gly27=
|
|
ENST00000498765.5:c.479G=
|
|
|
NM_000852.3:c.416G= , LRG_723t1:c.416G=
|
NP_000843.1:p.Gly139=
|
|
NM_000852.4:c.416G=
MANE Select
|
NP_000843.1:p.Gly139=
|
|