ENST00000426263.10:c.390T=
MANE Select
|
ENSP00000416293.2:p.Gly130=
|
|
ENST00000674765.1:c.390T=
|
ENSP00000501811.1:p.Gly130=
|
|
ENST00000675112.1:n.413T=
|
|
|
ENST00000676254.1:n.839T=
|
|
|
ENST00000372500.4:c.294T=
|
ENSP00000361578.4:p.Gly98=
|
|
ENST00000426263.7:c.390T=
|
ENSP00000416293.2:p.Gly130=
|
|
ENST00000439722.2:c.269T=
|
ENSP00000395521.2:n.269T=
|
|
ENST00000475162.3:c.289T=
|
|
|
ENST00000625233.2:n.598T=
|
|
|
ENST00000630287.2:c.390T=
|
ENSP00000486694.1:p.Gly130=
|
|
NM_006516.2:c.390T=
|
NP_006507.2:p.Gly130=
|
|
NM_006516.3:c.390T=
|
NP_006507.2:p.Gly130=
|
|
NM_006516.4:c.390T=
MANE Select
|
NP_006507.2:p.Gly130=
|
|