ENST00000382103.7:c.354C>A
MANE Select
|
ENSP00000371535.2:p.Thr118=
|
|
ENST00000680581.1:c.354C>A
|
ENSP00000506483.1:p.Thr118=
|
|
ENST00000680824.1:n.1570C>A
|
|
|
ENST00000681071.1:n.646C>A
|
|
|
ENST00000681166.1:n.1401C>A
|
|
|
ENST00000681341.1:n.1495C>A
|
|
|
ENST00000681640.1:n.448C>A
|
|
|
ENST00000681948.1:c.609C>A
|
ENSP00000505991.1:p.Thr203=
|
|
ENST00000358971.7:c.*152C>A
|
ENSP00000351857.3:n.*152C>A
|
|
ENST00000382103.6:c.354C>A
|
ENSP00000371535.2:p.Thr118=
|
|
ENST00000514585.5:c.*55C>A
|
ENSP00000421880.1:n.*55C>A
|
|
NM_016955.3:c.354C>A
|
NP_058651.3:p.Thr118=
|
|
XM_005248168.2:c.117C>A
|
XP_005248225.1:p.Thr39=
|
|
XM_006713965.2:c.174C>A
|
XP_006714028.1:p.Thr58=
|
|
XM_011513846.1:c.351C>A
|
XP_011512148.1:p.Thr117=
|
|
XM_011513847.1:c.321C>A
|
XP_011512149.1:p.Thr107=
|
|
XM_011513848.1:c.174C>A
|
XP_011512150.1:p.Thr58=
|
|
XM_011513846.2:c.351C>A
|
XP_011512148.1:p.Thr117=
|
|
XM_011513847.2:c.321C>A
|
XP_011512149.1:p.Thr107=
|
|
XM_017008277.1:c.609C>A
|
XP_016863766.1:p.Thr203=
|
|
XM_017008278.1:c.-70C>A
|
XP_016863767.1:n.-70C>A
|
|
NM_016955.4:c.354C>A
MANE Select
|
NP_058651.3:p.Thr118=
|
|