ENST00000426263.10:c.78T>C
MANE Select
|
ENSP00000416293.2:p.Phe26=
|
|
ENST00000674765.1:c.78T>C
|
ENSP00000501811.1:p.Phe26=
|
|
ENST00000675112.1:n.101T>C
|
|
|
ENST00000372500.4:c.19-12056T>C
|
ENSP00000361578.4:n.19-12056T>C
|
|
ENST00000415851.6:n.295T>C
|
|
|
ENST00000426263.7:c.78T>C
|
ENSP00000416293.2:p.Phe26=
|
|
ENST00000625233.2:n.286T>C
|
|
|
ENST00000628173.1:n.297T>C
|
|
|
ENST00000630287.2:c.78T>C
|
ENSP00000486694.1:p.Phe26=
|
|
ENST00000630821.1:n.295T>C
|
|
|
NM_006516.2:c.78T>C
|
NP_006507.2:p.Phe26=
|
|
NM_006516.3:c.78T>C
|
NP_006507.2:p.Phe26=
|
|
NM_006516.4:c.78T>C
MANE Select
|
NP_006507.2:p.Phe26=
|
|