ENST00000379644.9:c.1786C>G
MANE Select
|
ENSP00000368965.4:p.Gln596Glu
|
|
ENST00000379644.8:c.1786C>G
|
ENSP00000368965.4:p.Gln596Glu
|
|
ENST00000519705.1:n.1102C>G
|
|
|
ENST00000521576.1:c.937C>G
|
ENSP00000429029.1:p.Gln313Glu
|
|
NM_152419.2:c.1786C>G
|
NP_689632.2:p.Gln596Glu
|
|
XM_005273409.1:c.1897C>G
|
XP_005273466.1:p.Gln633Glu
|
|
XM_005273410.1:c.1873C>G
|
XP_005273467.1:p.Gln625Glu
|
|
XM_005273411.1:c.1705C>G
|
XP_005273468.1:p.Gln569Glu
|
|
NM_001363227.1:c.1873C>G
|
NP_001350156.1:p.Gln625Glu
|
|
NM_001363228.1:c.1594C>G
|
NP_001350157.1:p.Gln532Glu
|
|
NM_001363229.1:c.922C>G
|
NP_001350158.1:p.Gln308Glu
|
|
NM_152419.3:c.1786C>G
MANE Select
|
NP_689632.2:p.Gln596Glu
|
|
NM_001363227.2:c.1873C>G
|
NP_001350156.1:p.Gln625Glu
|
|
NM_001363228.2:c.1594C>G
|
NP_001350157.1:p.Gln532Glu
|
|
NM_001363229.2:c.922C>G
|
NP_001350158.1:p.Gln308Glu
|
|