ENST00000265724.8:c.3273A>G
|
ENSP00000265724.3:p.Ala1091=
|
|
ENST00000622132.5:c.3273A>G
MANE Select
|
ENSP00000478255.1:p.Ala1091=
|
|
ENST00000265724.7:c.3273A>G
|
ENSP00000265724.3:p.Ala1091=
|
|
ENST00000475929.5:n.429A>G
|
|
|
ENST00000488737.6:n.915A>G
|
|
|
ENST00000496821.5:n.901A>G
|
|
|
ENST00000543898.5:c.3081A>G
|
ENSP00000444095.1:p.Ala1027=
|
|
ENST00000622132.4:c.3273A>G
|
ENSP00000478255.1:p.Ala1091=
|
|
NM_000927.4:c.3273A>G
|
NP_000918.2:p.Ala1091=
|
|
NM_001348944.1:c.3273A>G
|
NP_001335873.1:p.Ala1091=
|
|
NM_001348945.1:c.3483A>G
|
NP_001335874.1:p.Ala1161=
|
|
NM_001348946.1:c.3273A>G
|
NP_001335875.1:p.Ala1091=
|
|
NM_001348946.2:c.3273A>G
MANE Select
|
NP_001335875.1:p.Ala1091=
|
|
NM_000927.5:c.3273A>G
|
NP_000918.2:p.Ala1091=
|
|
NM_001348944.2:c.3273A>G
|
NP_001335873.1:p.Ala1091=
|
|
NM_001348945.2:c.3483A>G
|
NP_001335874.1:p.Ala1161=
|
|