ENST00000309383.6:c.2134C>G
MANE Select
|
ENSP00000310649.1:p.Gln712Glu
|
|
ENST00000309383.5:c.2134C>G
|
ENSP00000310649.1:p.Gln712Glu
|
|
ENST00000326848.7:c.1219C>G
|
ENSP00000320853.7:p.Gln407Glu
|
|
ENST00000590333.5:c.2182C>G
|
ENSP00000468190.1:p.Gln728Glu
|
|
NM_032430.1:c.2134C>G
|
NP_115806.1:p.Gln712Glu
|
|
XM_005259327.2:c.1864C>G
|
XP_005259384.1:p.Gln622Glu
|
|
XM_011527395.1:c.1891C>G
|
XP_011525697.1:p.Gln631Glu
|
|
XR_430213.2:n.2117C>G
|
|
|
XM_005259327.3:c.1864C>G
|
XP_005259384.1:p.Gln622Glu
|
|
XM_011527395.2:c.1606C>G
|
XP_011525697.2:p.Gln536Glu
|
|
XM_024451739.1:c.1909C>G
|
XP_024307507.1:p.Gln637Glu
|
|
XR_430213.4:n.2415C>G
|
|
|
NM_032430.2:c.2134C>G
MANE Select
|
NP_115806.1:p.Gln712Glu
|
|