ENST00000382103.7:c.369G>C
MANE Select
|
ENSP00000371535.2:p.Leu123=
|
|
ENST00000680581.1:c.369G>C
|
ENSP00000506483.1:p.Leu123=
|
|
ENST00000680824.1:n.1585G>C
|
|
|
ENST00000681071.1:n.661G>C
|
|
|
ENST00000681166.1:n.1416G>C
|
|
|
ENST00000681341.1:n.1510G>C
|
|
|
ENST00000681640.1:n.463G>C
|
|
|
ENST00000681948.1:c.624G>C
|
ENSP00000505991.1:p.Leu208=
|
|
ENST00000358971.7:c.*167G>C
|
ENSP00000351857.3:n.*167G>C
|
|
ENST00000382103.6:c.369G>C
|
ENSP00000371535.2:p.Leu123=
|
|
ENST00000514585.5:c.*70G>C
|
ENSP00000421880.1:n.*70G>C
|
|
NM_016955.3:c.369G>C
|
NP_058651.3:p.Leu123=
|
|
XM_005248168.2:c.132G>C
|
XP_005248225.1:p.Leu44=
|
|
XM_006713965.2:c.189G>C
|
XP_006714028.1:p.Leu63=
|
|
XM_011513846.1:c.366G>C
|
XP_011512148.1:p.Leu122=
|
|
XM_011513847.1:c.336G>C
|
XP_011512149.1:p.Leu112=
|
|
XM_011513848.1:c.189G>C
|
XP_011512150.1:p.Leu63=
|
|
XM_011513846.2:c.366G>C
|
XP_011512148.1:p.Leu122=
|
|
XM_011513847.2:c.336G>C
|
XP_011512149.1:p.Leu112=
|
|
XM_017008277.1:c.624G>C
|
XP_016863766.1:p.Leu208=
|
|
XM_017008278.1:c.-55G>C
|
XP_016863767.1:n.-55G>C
|
|
NM_016955.4:c.369G>C
MANE Select
|
NP_058651.3:p.Leu123=
|
|