ENST00000381418.9:c.3426C>G
MANE Select
|
ENSP00000370826.4:p.Ser1142=
|
|
ENST00000680789.1:c.3426C>G
|
ENSP00000505181.1:p.Ser1142=
|
|
ENST00000312841.9:c.3261C>G
|
ENSP00000326765.8:p.Ser1087=
|
|
ENST00000381418.8:c.3426C>G
|
ENSP00000370826.4:p.Ser1142=
|
|
ENST00000522016.1:n.1619C>G
|
|
|
NM_005144.4:c.3426C>G
|
NP_005135.2:p.Ser1142=
|
|
NM_018411.4:c.3261C>G
|
NP_060881.2:p.Ser1087=
|
|
XM_005273569.1:c.3429C>G
|
XP_005273626.1:p.Ser1143=
|
|
XM_006716367.1:c.3264C>G
|
XP_006716430.1:p.Ser1088=
|
|
XM_005273569.2:c.3429C>G
|
XP_005273626.1:p.Ser1143=
|
|
XM_006716367.2:c.3264C>G
|
XP_006716430.1:p.Ser1088=
|
|
NM_005144.5:c.3426C>G
MANE Select
|
NP_005135.2:p.Ser1142=
|
|