ENST00000426263.10:c.381C>T
MANE Select
|
ENSP00000416293.2:p.Phe127=
|
|
ENST00000674765.1:c.381C>T
|
ENSP00000501811.1:p.Phe127=
|
|
ENST00000675112.1:n.404C>T
|
|
|
ENST00000676254.1:n.830C>T
|
|
|
ENST00000372500.4:c.285C>T
|
ENSP00000361578.4:p.Phe95=
|
|
ENST00000426263.7:c.381C>T
|
ENSP00000416293.2:p.Phe127=
|
|
ENST00000439722.2:c.260C>T
|
ENSP00000395521.2:n.260C>T
|
|
ENST00000475162.3:c.280C>T
|
|
|
ENST00000625233.2:n.589C>T
|
|
|
ENST00000630287.2:c.381C>T
|
ENSP00000486694.1:p.Phe127=
|
|
NM_006516.2:c.381C>T
|
NP_006507.2:p.Phe127=
|
|
NM_006516.3:c.381C>T
|
NP_006507.2:p.Phe127=
|
|
NM_006516.4:c.381C>T
MANE Select
|
NP_006507.2:p.Phe127=
|
|