ENST00000334232.9:c.309C>T
MANE Select
|
ENSP00000335076.4:p.Ser103=
|
|
ENST00000359362.6:c.279C>T
|
ENSP00000352320.4:p.Ser93=
|
|
ENST00000637660.1:c.243C>T
|
ENSP00000490347.1:p.Ser81=
|
|
ENST00000642595.1:c.236-9427C>T
|
ENSP00000494458.1:n.236-9427C>T
|
|
ENST00000334232.8:c.309C>T
|
ENSP00000335076.4:p.Ser103=
|
|
ENST00000359362.5:c.279C>T
|
ENSP00000352320.4:p.Ser93=
|
|
ENST00000439430.5:c.243C>T
|
ENSP00000405815.1:p.Ser81=
|
|
NM_080738.3:c.279C>T
|
NP_542776.1:p.Ser93=
|
|
NM_145861.2:c.309C>T
|
NP_665860.2:p.Ser103=
|
|
NM_080738.4:c.279C>T
|
NP_542776.1:p.Ser93=
|
|
NM_145861.4:c.309C>T
MANE Select
|
NP_665860.2:p.Ser103=
|
|