ENST00000449082.3:c.3109G>C
MANE Select
|
ENSP00000390600.2:p.Glu1037Gln
|
|
ENST00000643924.1:c.3106G>C
|
ENSP00000495595.1:p.Glu1036Gln
|
|
ENST00000655275.1:c.3133G>C
|
ENSP00000499510.1:p.Glu1045Gln
|
|
ENST00000449082.2:c.3109G>C
|
ENSP00000390600.2:p.Glu1037Gln
|
|
NM_001293306.2:c.3106G>C
|
NP_001280235.2:p.Glu1036Gln
|
|
NM_001293307.2:c.2815G>C
|
NP_001280236.2:p.Glu939Gln
|
|
NM_006514.3:c.3109G>C
|
NP_006505.3:p.Glu1037Gln
|
|
XM_005265371.2:c.3118G>C
|
XP_005265428.1:p.Glu1040Gln
|
|
XM_011533993.1:c.3115G>C
|
XP_011532295.1:p.Glu1039Gln
|
|
XM_011533994.1:c.2824G>C
|
XP_011532296.1:p.Glu942Gln
|
|
XM_005265371.3:c.3118G>C
|
XP_005265428.1:p.Glu1040Gln
|
|
XM_011533993.2:c.3115G>C
|
XP_011532295.1:p.Glu1039Gln
|
|
XM_011533994.2:c.2824G>C
|
XP_011532296.1:p.Glu942Gln
|
|
NM_006514.4:c.3109G>C
MANE Select
|
NP_006505.4:p.Glu1037Gln
|
|