ENST00000382103.7:c.993A>G
MANE Select
|
ENSP00000371535.2:p.Ser331=
|
|
ENST00000680581.1:c.993A>G
|
ENSP00000506483.1:p.Ser331=
|
|
ENST00000680824.1:n.2209A>G
|
|
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ENST00000681071.1:n.1285A>G
|
|
|
ENST00000681341.1:n.2134A>G
|
|
|
ENST00000681948.1:c.1248A>G
|
ENSP00000505991.1:p.Ser416=
|
|
ENST00000358971.7:c.*791A>G
|
ENSP00000351857.3:n.*791A>G
|
|
ENST00000382103.6:c.993A>G
|
ENSP00000371535.2:p.Ser331=
|
|
ENST00000503150.1:c.275A>G
|
|
|
ENST00000505513.1:n.293A>G
|
|
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ENST00000514585.5:c.*694A>G
|
ENSP00000421880.1:n.*694A>G
|
|
NM_016955.3:c.993A>G
|
NP_058651.3:p.Ser331=
|
|
XM_005248168.2:c.756A>G
|
XP_005248225.1:p.Ser252=
|
|
XM_006713965.2:c.813A>G
|
XP_006714028.1:p.Ser271=
|
|
XM_011513846.1:c.990A>G
|
XP_011512148.1:p.Ser330=
|
|
XM_011513847.1:c.960A>G
|
XP_011512149.1:p.Ser320=
|
|
XM_011513848.1:c.813A>G
|
XP_011512150.1:p.Ser271=
|
|
XM_011513846.2:c.990A>G
|
XP_011512148.1:p.Ser330=
|
|
XM_011513847.2:c.960A>G
|
XP_011512149.1:p.Ser320=
|
|
XM_017008277.1:c.1248A>G
|
XP_016863766.1:p.Ser416=
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|
XM_017008278.1:c.570A>G
|
XP_016863767.1:p.Ser190=
|
|
NM_016955.4:c.993A>G
MANE Select
|
NP_058651.3:p.Ser331=
|
|