ENST00000382103.7:c.384G>T
MANE Select
|
ENSP00000371535.2:p.Leu128=
|
|
ENST00000680581.1:c.384G>T
|
ENSP00000506483.1:p.Leu128=
|
|
ENST00000680824.1:n.1600G>T
|
|
|
ENST00000681071.1:n.676G>T
|
|
|
ENST00000681166.1:n.1431G>T
|
|
|
ENST00000681341.1:n.1525G>T
|
|
|
ENST00000681640.1:n.478G>T
|
|
|
ENST00000681948.1:c.639G>T
|
ENSP00000505991.1:p.Leu213=
|
|
ENST00000358971.7:c.*182G>T
|
ENSP00000351857.3:n.*182G>T
|
|
ENST00000382103.6:c.384G>T
|
ENSP00000371535.2:p.Leu128=
|
|
ENST00000514585.5:c.*85G>T
|
ENSP00000421880.1:n.*85G>T
|
|
NM_016955.3:c.384G>T
|
NP_058651.3:p.Leu128=
|
|
XM_005248168.2:c.147G>T
|
XP_005248225.1:p.Leu49=
|
|
XM_006713965.2:c.204G>T
|
XP_006714028.1:p.Leu68=
|
|
XM_011513846.1:c.381G>T
|
XP_011512148.1:p.Leu127=
|
|
XM_011513847.1:c.351G>T
|
XP_011512149.1:p.Leu117=
|
|
XM_011513848.1:c.204G>T
|
XP_011512150.1:p.Leu68=
|
|
XM_011513846.2:c.381G>T
|
XP_011512148.1:p.Leu127=
|
|
XM_011513847.2:c.351G>T
|
XP_011512149.1:p.Leu117=
|
|
XM_017008277.1:c.639G>T
|
XP_016863766.1:p.Leu213=
|
|
XM_017008278.1:c.-40G>T
|
XP_016863767.1:n.-40G>T
|
|
NM_016955.4:c.384G>T
MANE Select
|
NP_058651.3:p.Leu128=
|
|