ENST00000382103.7:c.982T>G
MANE Select
|
ENSP00000371535.2:p.Ser328Ala
|
|
ENST00000680581.1:c.982T>G
|
ENSP00000506483.1:p.Ser328Ala
|
|
ENST00000680824.1:n.2198T>G
|
|
|
ENST00000681071.1:n.1274T>G
|
|
|
ENST00000681341.1:n.2123T>G
|
|
|
ENST00000681948.1:c.1237T>G
|
ENSP00000505991.1:p.Ser413Ala
|
|
ENST00000358971.7:c.*780T>G
|
ENSP00000351857.3:n.*780T>G
|
|
ENST00000382103.6:c.982T>G
|
ENSP00000371535.2:p.Ser328Ala
|
|
ENST00000503150.1:c.264T>G
|
|
|
ENST00000505513.1:n.282T>G
|
|
|
ENST00000514585.5:c.*683T>G
|
ENSP00000421880.1:n.*683T>G
|
|
NM_016955.3:c.982T>G
|
NP_058651.3:p.Ser328Ala
|
|
XM_005248168.2:c.745T>G
|
XP_005248225.1:p.Ser249Ala
|
|
XM_006713965.2:c.802T>G
|
XP_006714028.1:p.Ser268Ala
|
|
XM_011513846.1:c.979T>G
|
XP_011512148.1:p.Ser327Ala
|
|
XM_011513847.1:c.949T>G
|
XP_011512149.1:p.Ser317Ala
|
|
XM_011513848.1:c.802T>G
|
XP_011512150.1:p.Ser268Ala
|
|
XM_011513846.2:c.979T>G
|
XP_011512148.1:p.Ser327Ala
|
|
XM_011513847.2:c.949T>G
|
XP_011512149.1:p.Ser317Ala
|
|
XM_017008277.1:c.1237T>G
|
XP_016863766.1:p.Ser413Ala
|
|
XM_017008278.1:c.559T>G
|
XP_016863767.1:p.Ser187Ala
|
|
NM_016955.4:c.982T>G
MANE Select
|
NP_058651.3:p.Ser328Ala
|
|