ENST00000334232.9:c.402A>G
MANE Select
|
ENSP00000335076.4:p.Pro134=
|
|
ENST00000359362.6:c.372A>G
|
ENSP00000352320.4:p.Pro124=
|
|
ENST00000637660.1:c.336A>G
|
ENSP00000490347.1:p.Pro112=
|
|
ENST00000642595.1:c.236-9334A>G
|
ENSP00000494458.1:n.236-9334A>G
|
|
ENST00000334232.8:c.402A>G
|
ENSP00000335076.4:p.Pro134=
|
|
ENST00000359362.5:c.372A>G
|
ENSP00000352320.4:p.Pro124=
|
|
NM_080738.3:c.372A>G
|
NP_542776.1:p.Pro124=
|
|
NM_145861.2:c.402A>G
|
NP_665860.2:p.Pro134=
|
|
NM_080738.4:c.372A>G
|
NP_542776.1:p.Pro124=
|
|
NM_145861.4:c.402A>G
MANE Select
|
NP_665860.2:p.Pro134=
|
|