ENST00000382103.7:c.941C>G
MANE Select
|
ENSP00000371535.2:p.Ala314Gly
|
|
ENST00000680581.1:c.941C>G
|
ENSP00000506483.1:p.Ala314Gly
|
|
ENST00000680824.1:n.2157C>G
|
|
|
ENST00000681071.1:n.1233C>G
|
|
|
ENST00000681341.1:n.2082C>G
|
|
|
ENST00000681948.1:c.1196C>G
|
ENSP00000505991.1:p.Ala399Gly
|
|
ENST00000358971.7:c.*739C>G
|
ENSP00000351857.3:n.*739C>G
|
|
ENST00000382103.6:c.941C>G
|
ENSP00000371535.2:p.Ala314Gly
|
|
ENST00000503150.1:c.223C>G
|
|
|
ENST00000505513.1:n.241C>G
|
|
|
ENST00000514585.5:c.*642C>G
|
ENSP00000421880.1:n.*642C>G
|
|
NM_016955.3:c.941C>G
|
NP_058651.3:p.Ala314Gly
|
|
XM_005248168.2:c.704C>G
|
XP_005248225.1:p.Ala235Gly
|
|
XM_006713965.2:c.761C>G
|
XP_006714028.1:p.Ala254Gly
|
|
XM_011513846.1:c.938C>G
|
XP_011512148.1:p.Ala313Gly
|
|
XM_011513847.1:c.908C>G
|
XP_011512149.1:p.Ala303Gly
|
|
XM_011513848.1:c.761C>G
|
XP_011512150.1:p.Ala254Gly
|
|
XM_011513846.2:c.938C>G
|
XP_011512148.1:p.Ala313Gly
|
|
XM_011513847.2:c.908C>G
|
XP_011512149.1:p.Ala303Gly
|
|
XM_017008277.1:c.1196C>G
|
XP_016863766.1:p.Ala399Gly
|
|
XM_017008278.1:c.518C>G
|
XP_016863767.1:p.Ala173Gly
|
|
NM_016955.4:c.941C>G
MANE Select
|
NP_058651.3:p.Ala314Gly
|
|