ENST00000265724.8:c.1242C>T
|
ENSP00000265724.3:p.Asn414=
|
|
ENST00000622132.5:c.1242C>T
MANE Select
|
ENSP00000478255.1:p.Asn414=
|
|
ENST00000265724.7:c.1242C>T
|
ENSP00000265724.3:p.Asn414=
|
|
ENST00000543898.5:c.1050C>T
|
ENSP00000444095.1:p.Asn350=
|
|
ENST00000622132.4:c.1242C>T
|
ENSP00000478255.1:p.Asn414=
|
|
NM_000927.4:c.1242C>T
|
NP_000918.2:p.Asn414=
|
|
NM_001348944.1:c.1242C>T
|
NP_001335873.1:p.Asn414=
|
|
NM_001348945.1:c.1452C>T
|
NP_001335874.1:p.Asn484=
|
|
NM_001348946.1:c.1242C>T
|
NP_001335875.1:p.Asn414=
|
|
NM_001348946.2:c.1242C>T
MANE Select
|
NP_001335875.1:p.Asn414=
|
|
NM_000927.5:c.1242C>T
|
NP_000918.2:p.Asn414=
|
|
NM_001348944.2:c.1242C>T
|
NP_001335873.1:p.Asn414=
|
|
NM_001348945.2:c.1452C>T
|
NP_001335874.1:p.Asn484=
|
|