ENST00000449082.3:c.3092A>T
MANE Select
|
ENSP00000390600.2:p.Glu1031Val
|
|
ENST00000643924.1:c.3089A>T
|
ENSP00000495595.1:p.Glu1030Val
|
|
ENST00000655275.1:c.3116A>T
|
ENSP00000499510.1:p.Glu1039Val
|
|
ENST00000449082.2:c.3092A>T
|
ENSP00000390600.2:p.Glu1031Val
|
|
NM_001293306.2:c.3089A>T
|
NP_001280235.2:p.Glu1030Val
|
|
NM_001293307.2:c.2798A>T
|
NP_001280236.2:p.Glu933Val
|
|
NM_006514.3:c.3092A>T
|
NP_006505.3:p.Glu1031Val
|
|
XM_005265371.2:c.3101A>T
|
XP_005265428.1:p.Glu1034Val
|
|
XM_011533993.1:c.3098A>T
|
XP_011532295.1:p.Glu1033Val
|
|
XM_011533994.1:c.2807A>T
|
XP_011532296.1:p.Glu936Val
|
|
XM_005265371.3:c.3101A>T
|
XP_005265428.1:p.Glu1034Val
|
|
XM_011533993.2:c.3098A>T
|
XP_011532295.1:p.Glu1033Val
|
|
XM_011533994.2:c.2807A>T
|
XP_011532296.1:p.Glu936Val
|
|
NM_006514.4:c.3092A>T
MANE Select
|
NP_006505.4:p.Glu1031Val
|
|