ENST00000449082.3:c.3188A>C
MANE Select
|
ENSP00000390600.2:p.Glu1063Ala
|
|
ENST00000643924.1:c.3185A>C
|
ENSP00000495595.1:p.Glu1062Ala
|
|
ENST00000655275.1:c.3212A>C
|
ENSP00000499510.1:p.Glu1071Ala
|
|
ENST00000449082.2:c.3188A>C
|
ENSP00000390600.2:p.Glu1063Ala
|
|
NM_001293306.2:c.3185A>C
|
NP_001280235.2:p.Glu1062Ala
|
|
NM_001293307.2:c.2894A>C
|
NP_001280236.2:p.Glu965Ala
|
|
NM_006514.3:c.3188A>C
|
NP_006505.3:p.Glu1063Ala
|
|
XM_005265371.2:c.3197A>C
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XP_005265428.1:p.Glu1066Ala
|
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XM_011533993.1:c.3194A>C
|
XP_011532295.1:p.Glu1065Ala
|
|
XM_011533994.1:c.2903A>C
|
XP_011532296.1:p.Glu968Ala
|
|
XM_005265371.3:c.3197A>C
|
XP_005265428.1:p.Glu1066Ala
|
|
XM_011533993.2:c.3194A>C
|
XP_011532295.1:p.Glu1065Ala
|
|
XM_011533994.2:c.2903A>C
|
XP_011532296.1:p.Glu968Ala
|
|
NM_006514.4:c.3188A>C
MANE Select
|
NP_006505.4:p.Glu1063Ala
|
|