ENST00000382103.7:c.357T>G
MANE Select
|
ENSP00000371535.2:p.Asn119Lys
|
|
ENST00000680581.1:c.357T>G
|
ENSP00000506483.1:p.Asn119Lys
|
|
ENST00000680824.1:n.1573T>G
|
|
|
ENST00000681071.1:n.649T>G
|
|
|
ENST00000681166.1:n.1404T>G
|
|
|
ENST00000681341.1:n.1498T>G
|
|
|
ENST00000681640.1:n.451T>G
|
|
|
ENST00000681948.1:c.612T>G
|
ENSP00000505991.1:p.Asn204Lys
|
|
ENST00000358971.7:c.*155T>G
|
ENSP00000351857.3:n.*155T>G
|
|
ENST00000382103.6:c.357T>G
|
ENSP00000371535.2:p.Asn119Lys
|
|
ENST00000514585.5:c.*58T>G
|
ENSP00000421880.1:n.*58T>G
|
|
NM_016955.3:c.357T>G
|
NP_058651.3:p.Asn119Lys
|
|
XM_005248168.2:c.120T>G
|
XP_005248225.1:p.Asn40Lys
|
|
XM_006713965.2:c.177T>G
|
XP_006714028.1:p.Asn59Lys
|
|
XM_011513846.1:c.354T>G
|
XP_011512148.1:p.Asn118Lys
|
|
XM_011513847.1:c.324T>G
|
XP_011512149.1:p.Asn108Lys
|
|
XM_011513848.1:c.177T>G
|
XP_011512150.1:p.Asn59Lys
|
|
XM_011513846.2:c.354T>G
|
XP_011512148.1:p.Asn118Lys
|
|
XM_011513847.2:c.324T>G
|
XP_011512149.1:p.Asn108Lys
|
|
XM_017008277.1:c.612T>G
|
XP_016863766.1:p.Asn204Lys
|
|
XM_017008278.1:c.-67T>G
|
XP_016863767.1:n.-67T>G
|
|
NM_016955.4:c.357T>G
MANE Select
|
NP_058651.3:p.Asn119Lys
|
|