ENST00000382103.7:c.959T>A
MANE Select
|
ENSP00000371535.2:p.Leu320Ter
|
|
ENST00000680581.1:c.959T>A
|
ENSP00000506483.1:p.Leu320Ter
|
|
ENST00000680824.1:n.2175T>A
|
|
|
ENST00000681071.1:n.1251T>A
|
|
|
ENST00000681341.1:n.2100T>A
|
|
|
ENST00000681948.1:c.1214T>A
|
ENSP00000505991.1:p.Leu405Ter
|
|
ENST00000358971.7:c.*757T>A
|
ENSP00000351857.3:n.*757T>A
|
|
ENST00000382103.6:c.959T>A
|
ENSP00000371535.2:p.Leu320Ter
|
|
ENST00000503150.1:c.241T>A
|
|
|
ENST00000505513.1:n.259T>A
|
|
|
ENST00000514585.5:c.*660T>A
|
ENSP00000421880.1:n.*660T>A
|
|
NM_016955.3:c.959T>A
|
NP_058651.3:p.Leu320Ter
|
|
XM_005248168.2:c.722T>A
|
XP_005248225.1:p.Leu241Ter
|
|
XM_006713965.2:c.779T>A
|
XP_006714028.1:p.Leu260Ter
|
|
XM_011513846.1:c.956T>A
|
XP_011512148.1:p.Leu319Ter
|
|
XM_011513847.1:c.926T>A
|
XP_011512149.1:p.Leu309Ter
|
|
XM_011513848.1:c.779T>A
|
XP_011512150.1:p.Leu260Ter
|
|
XM_011513846.2:c.956T>A
|
XP_011512148.1:p.Leu319Ter
|
|
XM_011513847.2:c.926T>A
|
XP_011512149.1:p.Leu309Ter
|
|
XM_017008277.1:c.1214T>A
|
XP_016863766.1:p.Leu405Ter
|
|
XM_017008278.1:c.536T>A
|
XP_016863767.1:p.Leu179Ter
|
|
NM_016955.4:c.959T>A
MANE Select
|
NP_058651.3:p.Leu320Ter
|
|