ENST00000449082.3:c.3110A>T
MANE Select
|
ENSP00000390600.2:p.Glu1037Val
|
|
ENST00000643924.1:c.3107A>T
|
ENSP00000495595.1:p.Glu1036Val
|
|
ENST00000655275.1:c.3134A>T
|
ENSP00000499510.1:p.Glu1045Val
|
|
ENST00000449082.2:c.3110A>T
|
ENSP00000390600.2:p.Glu1037Val
|
|
NM_001293306.2:c.3107A>T
|
NP_001280235.2:p.Glu1036Val
|
|
NM_001293307.2:c.2816A>T
|
NP_001280236.2:p.Glu939Val
|
|
NM_006514.3:c.3110A>T
|
NP_006505.3:p.Glu1037Val
|
|
XM_005265371.2:c.3119A>T
|
XP_005265428.1:p.Glu1040Val
|
|
XM_011533993.1:c.3116A>T
|
XP_011532295.1:p.Glu1039Val
|
|
XM_011533994.1:c.2825A>T
|
XP_011532296.1:p.Glu942Val
|
|
XM_005265371.3:c.3119A>T
|
XP_005265428.1:p.Glu1040Val
|
|
XM_011533993.2:c.3116A>T
|
XP_011532295.1:p.Glu1039Val
|
|
XM_011533994.2:c.2825A>T
|
XP_011532296.1:p.Glu942Val
|
|
NM_006514.4:c.3110A>T
MANE Select
|
NP_006505.4:p.Glu1037Val
|
|