ENST00000612619.2:c.120G=
|
ENSP00000479970.1:p.Ala40=
|
|
ENST00000694948.1:n.218G=
|
|
|
ENST00000694949.1:n.215G=
|
|
|
ENST00000694950.1:c.200G=
|
|
|
ENST00000319363.11:c.120G=
MANE Select
|
ENSP00000320936.6:p.Ala40=
|
|
ENST00000319363.10:c.120G=
|
ENSP00000320936.6:p.Ala40=
|
|
ENST00000459971.1:n.155G=
|
|
|
ENST00000477874.1:n.258G=
|
|
|
ENST00000612619.1:c.120G=
|
ENSP00000479970.1:p.Ala40=
|
|
NM_001289905.1:c.120G=
|
NP_001276834.1:p.Ala40=
|
|
NM_014339.6:c.120G= , LRG_355t1:c.120G=
|
NP_055154.3:p.Ala40=
|
|
NM_014339.7:c.120G=
MANE Select
|
NP_055154.3:p.Ala40=
|
|
NM_001289905.2:c.120G=
|
NP_001276834.1:p.Ala40=
|
|