ENST00000355832.10:c.3207T>G
MANE Select
|
ENSP00000348089.5:p.Ser1069=
|
|
ENST00000679552.1:n.278T>G
|
|
|
ENST00000679871.1:n.353T>G
|
|
|
ENST00000679974.1:n.256T>G
|
|
|
ENST00000681632.1:n.4610T>G
|
|
|
ENST00000681659.1:c.3048T>G
|
ENSP00000505631.1:p.Ser1016=
|
|
ENST00000355832.9:c.3207T>G
|
ENSP00000348089.5:p.Ser1069=
|
|
ENST00000623073.3:c.*1503T>G
|
ENSP00000485650.1:n.*1503T>G
|
|
ENST00000623115.3:c.1317T>G
|
ENSP00000485321.1:p.Ser439=
|
|
ENST00000624341.3:c.1039T>G
|
|
|
NM_000124.3:c.3207T>G
|
NP_000115.1:p.Ser1069=
|
|
XR_945953.1:n.243-812A>C
|
|
|
NM_001346440.1:c.3207T>G
|
NP_001333369.1:p.Ser1069=
|
|
NM_000124.4:c.3207T>G
MANE Select
|
NP_000115.1:p.Ser1069=
|
|
NM_001346440.2:c.3207T>G
|
NP_001333369.1:p.Ser1069=
|
|