ENST00000305046.13:c.1107C>A
MANE Select
|
ENSP00000306606.8:p.Ile369=
|
|
ENST00000639454.1:c.1107C>A
|
ENSP00000491622.1:p.Ile369=
|
|
ENST00000305046.12:c.1107C>A
|
ENSP00000306606.8:p.Ile369=
|
|
ENST00000506651.5:c.987C>A
|
ENSP00000425998.2:p.Ile329=
|
|
ENST00000515694.4:n.3202C>A
|
|
|
ENST00000625860.2:c.987C>A
|
ENSP00000486614.1:p.Ile329=
|
|
NM_000668.5:c.1107C>A
|
NP_000659.2:p.Ile369=
|
|
NM_001286650.1:c.987C>A
|
NP_001273579.1:p.Ile329=
|
|
NM_000668.6:c.1107C>A
MANE Select
|
NP_000659.2:p.Ile369=
|
|
NM_001286650.2:c.987C>A
|
NP_001273579.1:p.Ile329=
|
|