ENST00000267890.11:c.3620A>G
MANE Select
|
ENSP00000267890.6:p.Glu1207Gly
|
|
ENST00000267890.10:c.3620A>G
|
ENSP00000267890.6:p.Glu1207Gly
|
|
ENST00000622375.4:c.4835A>G
|
ENSP00000479984.1:p.Glu1612Gly
|
|
NM_173500.3:c.3620A>G
|
NP_775771.3:p.Glu1207Gly
|
|
XM_005254171.3:c.3638A>G
|
XP_005254228.1:p.Glu1213Gly
|
|
XM_005254173.3:c.3413A>G
|
XP_005254230.1:p.Glu1138Gly
|
|
XM_006720402.2:c.3605A>G
|
XP_006720465.1:p.Glu1202Gly
|
|
XM_006720403.2:c.3413A>G
|
XP_006720466.1:p.Glu1138Gly
|
|
XM_011521267.1:c.3413A>G
|
XP_011519569.1:p.Glu1138Gly
|
|
XM_011521268.1:c.3353A>G
|
XP_011519570.1:p.Glu1118Gly
|
|
XM_011521269.1:c.3341A>G
|
XP_011519571.1:p.Glu1114Gly
|
|
XM_005254171.5:c.3638A>G
|
XP_005254228.1:p.Glu1213Gly
|
|
XM_005254173.5:c.3413A>G
|
XP_005254230.1:p.Glu1138Gly
|
|
XM_006720402.4:c.3605A>G
|
XP_006720465.1:p.Glu1202Gly
|
|
XM_006720403.4:c.3413A>G
|
XP_006720466.1:p.Glu1138Gly
|
|
XM_017021950.2:c.3341A>G
|
XP_016877439.1:p.Glu1114Gly
|
|
XM_024449849.1:c.3620A>G
|
XP_024305617.1:p.Glu1207Gly
|
|
XM_024449850.1:c.3620A>G
|
XP_024305618.1:p.Glu1207Gly
|
|
XM_024449851.1:c.3413A>G
|
XP_024305619.1:p.Glu1138Gly
|
|
NM_173500.4:c.3620A>G
MANE Select
|
NP_775771.3:p.Glu1207Gly
|
|