ENST00000382103.7:c.969T>G
MANE Select
|
ENSP00000371535.2:p.Leu323=
|
|
ENST00000680581.1:c.969T>G
|
ENSP00000506483.1:p.Leu323=
|
|
ENST00000680824.1:n.2185T>G
|
|
|
ENST00000681071.1:n.1261T>G
|
|
|
ENST00000681341.1:n.2110T>G
|
|
|
ENST00000681948.1:c.1224T>G
|
ENSP00000505991.1:p.Leu408=
|
|
ENST00000358971.7:c.*767T>G
|
ENSP00000351857.3:n.*767T>G
|
|
ENST00000382103.6:c.969T>G
|
ENSP00000371535.2:p.Leu323=
|
|
ENST00000503150.1:c.251T>G
|
|
|
ENST00000505513.1:n.269T>G
|
|
|
ENST00000514585.5:c.*670T>G
|
ENSP00000421880.1:n.*670T>G
|
|
NM_016955.3:c.969T>G
|
NP_058651.3:p.Leu323=
|
|
XM_005248168.2:c.732T>G
|
XP_005248225.1:p.Leu244=
|
|
XM_006713965.2:c.789T>G
|
XP_006714028.1:p.Leu263=
|
|
XM_011513846.1:c.966T>G
|
XP_011512148.1:p.Leu322=
|
|
XM_011513847.1:c.936T>G
|
XP_011512149.1:p.Leu312=
|
|
XM_011513848.1:c.789T>G
|
XP_011512150.1:p.Leu263=
|
|
XM_011513846.2:c.966T>G
|
XP_011512148.1:p.Leu322=
|
|
XM_011513847.2:c.936T>G
|
XP_011512149.1:p.Leu312=
|
|
XM_017008277.1:c.1224T>G
|
XP_016863766.1:p.Leu408=
|
|
XM_017008278.1:c.546T>G
|
XP_016863767.1:p.Leu182=
|
|
NM_016955.4:c.969T>G
MANE Select
|
NP_058651.3:p.Leu323=
|
|