ENST00000311907.10:c.712G=
MANE Select
|
ENSP00000308541.5:p.Ala238=
|
|
ENST00000311907.9:c.712G=
|
ENSP00000308541.5:p.Ala238=
|
|
ENST00000442468.1:c.682G=
|
ENSP00000387413.1:p.Ala228=
|
|
ENST00000490274.1:n.492G=
|
|
|
ENST00000530231.5:c.712G=
|
ENSP00000433907.1:p.Ala238=
|
|
NM_000506.3:c.712G=
|
NP_000497.1:p.Ala238=
|
|
NM_000506.4:c.712G= , LRG_551t1:c.712G=
|
NP_000497.1:p.Ala238=
|
|
NM_001311257.1:c.664G=
|
NP_001298186.1:p.Ala222=
|
|
XR_428840.2:n.756G=
|
|
|
XR_428840.4:n.747G=
|
|
|
NM_000506.5:c.712G=
MANE Select
|
NP_000497.1:p.Ala238=
|
|
NM_001311257.2:c.664G=
|
NP_001298186.1:p.Ala222=
|
|