ENST00000298139.7:c.3201A>T
MANE Select
|
ENSP00000298139.5:p.Glu1067Asp
|
|
ENST00000650667.1:c.*2815A>T
|
ENSP00000498593.1:n.*2815A>T
|
|
ENST00000298139.5:c.3201A>T
|
ENSP00000298139.5:p.Glu1067Asp
|
|
ENST00000521620.5:n.1834A>T
|
|
|
NM_000553.4:c.3201A>T , LRG_524t1:c.3201A>T
|
NP_000544.2:p.Glu1067Asp
|
|
XM_011544639.1:c.3120A>T
|
XP_011542941.1:p.Glu1040Asp
|
|
XM_011544640.1:c.1602A>T
|
XP_011542942.1:p.Glu534Asp
|
|
XR_949470.1:n.3474A>T
|
|
|
XR_949471.1:n.3474A>T
|
|
|
XR_949472.1:n.3474A>T
|
|
|
NM_000553.5:c.3201A>T
|
NP_000544.2:p.Glu1067Asp
|
|
XM_011544639.3:c.3120A>T
|
XP_011542941.1:p.Glu1040Asp
|
|
XM_024447265.1:c.2991A>T
|
XP_024303033.1:p.Glu997Asp
|
|
XR_949470.3:n.3502A>T
|
|
|
XR_949471.3:n.3502A>T
|
|
|
XR_949472.3:n.3502A>T
|
|
|
NM_000553.6:c.3201A>T
MANE Select
|
NP_000544.2:p.Glu1067Asp
|
|