ENST00000382103.7:c.1014A>T
MANE Select
|
ENSP00000371535.2:p.Leu338=
|
|
ENST00000680581.1:c.1014A>T
|
ENSP00000506483.1:p.Leu338=
|
|
ENST00000680824.1:n.2230A>T
|
|
|
ENST00000681071.1:n.1306A>T
|
|
|
ENST00000681341.1:n.2155A>T
|
|
|
ENST00000681948.1:c.1269A>T
|
ENSP00000505991.1:p.Leu423=
|
|
ENST00000358971.7:c.*812A>T
|
ENSP00000351857.3:n.*812A>T
|
|
ENST00000382103.6:c.1014A>T
|
ENSP00000371535.2:p.Leu338=
|
|
ENST00000503150.1:c.296A>T
|
|
|
ENST00000505513.1:n.314A>T
|
|
|
ENST00000514585.5:c.*715A>T
|
ENSP00000421880.1:n.*715A>T
|
|
NM_016955.3:c.1014A>T
|
NP_058651.3:p.Leu338=
|
|
XM_005248168.2:c.777A>T
|
XP_005248225.1:p.Leu259=
|
|
XM_006713965.2:c.834A>T
|
XP_006714028.1:p.Leu278=
|
|
XM_011513846.1:c.1011A>T
|
XP_011512148.1:p.Leu337=
|
|
XM_011513847.1:c.981A>T
|
XP_011512149.1:p.Leu327=
|
|
XM_011513848.1:c.834A>T
|
XP_011512150.1:p.Leu278=
|
|
XM_011513846.2:c.1011A>T
|
XP_011512148.1:p.Leu337=
|
|
XM_011513847.2:c.981A>T
|
XP_011512149.1:p.Leu327=
|
|
XM_017008277.1:c.1269A>T
|
XP_016863766.1:p.Leu423=
|
|
XM_017008278.1:c.591A>T
|
XP_016863767.1:p.Leu197=
|
|
NM_016955.4:c.1014A>T
MANE Select
|
NP_058651.3:p.Leu338=
|
|