ENST00000518377.3:c.104A>G
(HRURF)
MANE Select
|
ENSP00000505144.1:p.Ter35Trp
|
|
ENST00000381418.9:c.-218A>G
(HR)
MANE Select
|
ENSP00000370826.4:n.-218A>G
|
|
ENST00000518377.2:c.104A>G
(HRURF)
|
ENSP00000505144.1:p.Ter35Trp
|
|
ENST00000680789.1:c.-218A>G
(HR)
|
ENSP00000505181.1:n.-218A>G
|
|
ENST00000312841.9:c.-218A>G
(HR)
|
ENSP00000326765.8:n.-218A>G
|
|
ENST00000381418.8:c.-218A>G
(HR)
|
ENSP00000370826.4:n.-218A>G
|
|
ENST00000518377.1:n.570A>G
(HR)
|
|
|
ENST00000522759.1:n.77A>G
(HR)
|
|
|
NM_005144.4:c.-218A>G
(HR)
|
NP_005135.2:n.-218A>G
|
|
NM_018411.4:c.-218A>G
(HR)
|
NP_060881.2:n.-218A>G
|
|
XM_005273569.1:c.-218A>G
(HR)
|
XP_005273626.1:n.-218A>G
|
|
XM_006716367.1:c.-218A>G
(HR)
|
XP_006716430.1:n.-218A>G
|
|
XM_005273569.2:c.-218A>G
(HR)
|
XP_005273626.1:n.-218A>G
|
|
XM_006716367.2:c.-218A>G
(HR)
|
XP_006716430.1:n.-218A>G
|
|
NM_001394132.1:c.104A>G
(HRURF)
MANE Select
|
NP_001381061.1:p.Ter35Trp
|
|
NM_005144.5:c.-218A>G
(HR)
MANE Select
|
NP_005135.2:n.-218A>G
|
|