ENST00000367435.5:c.466C>A
MANE Select
|
ENSP00000356405.4:p.Arg156Ser
|
|
ENST00000635846.1:c.466C>A
|
ENSP00000490035.1:p.Arg156Ser
|
|
ENST00000643006.1:c.466C>A
|
ENSP00000496633.1:p.Arg156Ser
|
|
ENST00000643784.1:c.466C>A
|
ENSP00000494944.1:p.Arg156Ser
|
|
ENST00000647662.1:n.367C>A
|
|
|
ENST00000648071.1:c.*442C>A
|
ENSP00000497513.1:n.*442C>A
|
|
ENST00000649606.1:n.479C>A
|
|
|
ENST00000649706.1:n.407C>A
|
|
|
ENST00000649895.1:n.684C>A
|
|
|
ENST00000650197.1:c.466C>A
|
ENSP00000496929.1:p.Arg156Ser
|
|
ENST00000367435.3:c.466C>A
|
ENSP00000356405.3:p.Arg156Ser
|
|
ENST00000482484.1:n.718C>A
|
|
|
NM_024529.4:c.466C>A , LRG_507t1:c.466C>A
|
NP_078805.3:p.Arg156Ser
|
|
XM_006711537.2:c.466C>A
|
XP_006711600.1:p.Arg156Ser
|
|
XM_006711537.4:c.466C>A
|
XP_006711600.1:p.Arg156Ser
|
|
NM_024529.5:c.466C>A
MANE Select
|
NP_078805.3:p.Arg156Ser
|
|