ENST00000382103.7:c.1000T>G
MANE Select
|
ENSP00000371535.2:p.Tyr334Asp
|
|
ENST00000680581.1:c.1000T>G
|
ENSP00000506483.1:p.Tyr334Asp
|
|
ENST00000680824.1:n.2216T>G
|
|
|
ENST00000681071.1:n.1292T>G
|
|
|
ENST00000681341.1:n.2141T>G
|
|
|
ENST00000681948.1:c.1255T>G
|
ENSP00000505991.1:p.Tyr419Asp
|
|
ENST00000358971.7:c.*798T>G
|
ENSP00000351857.3:n.*798T>G
|
|
ENST00000382103.6:c.1000T>G
|
ENSP00000371535.2:p.Tyr334Asp
|
|
ENST00000503150.1:c.282T>G
|
|
|
ENST00000505513.1:n.300T>G
|
|
|
ENST00000514585.5:c.*701T>G
|
ENSP00000421880.1:n.*701T>G
|
|
NM_016955.3:c.1000T>G
|
NP_058651.3:p.Tyr334Asp
|
|
XM_005248168.2:c.763T>G
|
XP_005248225.1:p.Tyr255Asp
|
|
XM_006713965.2:c.820T>G
|
XP_006714028.1:p.Tyr274Asp
|
|
XM_011513846.1:c.997T>G
|
XP_011512148.1:p.Tyr333Asp
|
|
XM_011513847.1:c.967T>G
|
XP_011512149.1:p.Tyr323Asp
|
|
XM_011513848.1:c.820T>G
|
XP_011512150.1:p.Tyr274Asp
|
|
XM_011513846.2:c.997T>G
|
XP_011512148.1:p.Tyr333Asp
|
|
XM_011513847.2:c.967T>G
|
XP_011512149.1:p.Tyr323Asp
|
|
XM_017008277.1:c.1255T>G
|
XP_016863766.1:p.Tyr419Asp
|
|
XM_017008278.1:c.577T>G
|
XP_016863767.1:p.Tyr193Asp
|
|
NM_016955.4:c.1000T>G
MANE Select
|
NP_058651.3:p.Tyr334Asp
|
|