NM_012335.4:c.2508G>T
MANE Select
|
NP_036467.2:p.Glu836Asp
|
ENST00000644032.2:c.2508G>T
MANE Select
|
ENSP00000494550.1:p.Glu836Asp
|
NM_001348355.1:c.2496G>T
|
NP_001335284.1:p.Glu832Asp
|
NM_001348355.2:c.2496G>T
|
NP_001335284.1:p.Glu832Asp
|
NM_012335.3:c.2508G>T
|
NP_036467.2:p.Glu836Asp
|
ENST00000338257.12:c.2508G>T
|
ENSP00000344871.6:p.Glu836Asp
|
ENST00000598005.1:c.991G>T
|
ENSP00000469098.1:n.991G>T
|
ENST00000600885.1:n.84G>T
|
|
ENST00000613525.4:c.2508G>T
|
ENSP00000481682.1:p.Glu836Asp
|
XM_011528024.1:c.2571G>T
|
XP_011526326.1:p.Glu857Asp
|
XM_011528024.2:c.2571G>T
|
XP_011526326.1:p.Glu857Asp
|
XM_011528025.1:c.2559G>T
|
XP_011526327.1:p.Glu853Asp
|
XM_011528025.2:c.2559G>T
|
XP_011526327.1:p.Glu853Asp
|
XM_011528026.1:c.2484G>T
|
XP_011526328.1:p.Glu828Asp
|
XM_011528026.2:c.2484G>T
|
XP_011526328.1:p.Glu828Asp
|
XM_011528027.1:c.2436G>T
|
XP_011526329.1:p.Glu812Asp
|
XM_011528027.2:c.2436G>T
|
XP_011526329.1:p.Glu812Asp
|
XM_024451522.1:c.1353G>T
|
XP_024307290.1:p.Glu451Asp
|
XR_001753692.2:n.2690G>T
|
|
XR_936179.1:n.2695G>T
|
|