ENST00000382103.7:c.950C>A
MANE Select
|
ENSP00000371535.2:p.Ser317Ter
|
|
ENST00000680581.1:c.950C>A
|
ENSP00000506483.1:p.Ser317Ter
|
|
ENST00000680824.1:n.2166C>A
|
|
|
ENST00000681071.1:n.1242C>A
|
|
|
ENST00000681341.1:n.2091C>A
|
|
|
ENST00000681948.1:c.1205C>A
|
ENSP00000505991.1:p.Ser402Ter
|
|
ENST00000358971.7:c.*748C>A
|
ENSP00000351857.3:n.*748C>A
|
|
ENST00000382103.6:c.950C>A
|
ENSP00000371535.2:p.Ser317Ter
|
|
ENST00000503150.1:c.232C>A
|
|
|
ENST00000505513.1:n.250C>A
|
|
|
ENST00000514585.5:c.*651C>A
|
ENSP00000421880.1:n.*651C>A
|
|
NM_016955.3:c.950C>A
|
NP_058651.3:p.Ser317Ter
|
|
XM_005248168.2:c.713C>A
|
XP_005248225.1:p.Ser238Ter
|
|
XM_006713965.2:c.770C>A
|
XP_006714028.1:p.Ser257Ter
|
|
XM_011513846.1:c.947C>A
|
XP_011512148.1:p.Ser316Ter
|
|
XM_011513847.1:c.917C>A
|
XP_011512149.1:p.Ser306Ter
|
|
XM_011513848.1:c.770C>A
|
XP_011512150.1:p.Ser257Ter
|
|
XM_011513846.2:c.947C>A
|
XP_011512148.1:p.Ser316Ter
|
|
XM_011513847.2:c.917C>A
|
XP_011512149.1:p.Ser306Ter
|
|
XM_017008277.1:c.1205C>A
|
XP_016863766.1:p.Ser402Ter
|
|
XM_017008278.1:c.527C>A
|
XP_016863767.1:p.Ser176Ter
|
|
NM_016955.4:c.950C>A
MANE Select
|
NP_058651.3:p.Ser317Ter
|
|