ENST00000426263.10:c.99C>T
MANE Select
|
ENSP00000416293.2:p.Ile33=
|
|
ENST00000674765.1:c.99C>T
|
ENSP00000501811.1:p.Ile33=
|
|
ENST00000675112.1:n.122C>T
|
|
|
ENST00000372500.4:c.19-12035C>T
|
ENSP00000361578.4:n.19-12035C>T
|
|
ENST00000415851.6:n.316C>T
|
|
|
ENST00000426263.7:c.99C>T
|
ENSP00000416293.2:p.Ile33=
|
|
ENST00000625233.2:n.307C>T
|
|
|
ENST00000628173.1:n.318C>T
|
|
|
ENST00000630287.2:c.99C>T
|
ENSP00000486694.1:p.Ile33=
|
|
ENST00000630821.1:n.316C>T
|
|
|
NM_006516.2:c.99C>T
|
NP_006507.2:p.Ile33=
|
|
NM_006516.3:c.99C>T
|
NP_006507.2:p.Ile33=
|
|
NM_006516.4:c.99C>T
MANE Select
|
NP_006507.2:p.Ile33=
|
|