ENST00000321612.8:c.2029G=
MANE Select
|
ENSP00000370737.4:p.Asp677=
|
|
ENST00000460457.2:n.189G=
|
|
|
ENST00000638233.1:n.464G=
|
|
|
ENST00000638661.1:c.229G=
|
ENSP00000491369.1:p.Asp77=
|
|
ENST00000638694.1:n.216G=
|
|
|
ENST00000639318.1:c.229G=
|
ENSP00000491932.1:p.Asp77=
|
|
ENST00000639364.1:n.1729G=
|
|
|
ENST00000639443.1:n.1597G=
|
|
|
ENST00000639954.1:n.1737G=
|
|
|
ENST00000640208.1:c.229G=
|
ENSP00000491895.1:p.Asp77=
|
|
ENST00000640505.1:n.268G=
|
|
|
ENST00000640592.1:n.1912G=
|
|
|
ENST00000321612.6:c.2029G=
|
ENSP00000370737.3:p.Asp677=
|
|
ENST00000460457.1:n.168G=
|
|
|
NM_000170.2:c.2029G= , LRG_643t1:c.2029G=
|
NP_000161.2:p.Asp677=
|
|
NM_000170.3:c.2029G=
MANE Select
|
NP_000161.2:p.Asp677=
|
|