ENST00000382103.7:c.365T=
MANE Select
|
ENSP00000371535.2:p.Val122=
|
|
ENST00000680581.1:c.365T=
|
ENSP00000506483.1:p.Val122=
|
|
ENST00000680824.1:n.1581T=
|
|
|
ENST00000681071.1:n.657T=
|
|
|
ENST00000681166.1:n.1412T=
|
|
|
ENST00000681341.1:n.1506T=
|
|
|
ENST00000681640.1:n.459T=
|
|
|
ENST00000681948.1:c.620T=
|
ENSP00000505991.1:p.Val207=
|
|
ENST00000358971.7:c.*163T=
|
ENSP00000351857.3:n.*163T=
|
|
ENST00000382103.6:c.365T=
|
ENSP00000371535.2:p.Val122=
|
|
ENST00000514585.5:c.*66T=
|
ENSP00000421880.1:n.*66T=
|
|
NM_016955.3:c.365T=
|
NP_058651.3:p.Val122=
|
|
XM_005248168.2:c.128T=
|
XP_005248225.1:p.Val43=
|
|
XM_006713965.2:c.185T=
|
XP_006714028.1:p.Val62=
|
|
XM_011513846.1:c.362T=
|
XP_011512148.1:p.Val121=
|
|
XM_011513847.1:c.332T=
|
XP_011512149.1:p.Val111=
|
|
XM_011513848.1:c.185T=
|
XP_011512150.1:p.Val62=
|
|
XM_011513846.2:c.362T=
|
XP_011512148.1:p.Val121=
|
|
XM_011513847.2:c.332T=
|
XP_011512149.1:p.Val111=
|
|
XM_017008277.1:c.620T=
|
XP_016863766.1:p.Val207=
|
|
XM_017008278.1:c.-59T=
|
XP_016863767.1:n.-59T=
|
|
NM_016955.4:c.365T=
MANE Select
|
NP_058651.3:p.Val122=
|
|