ENST00000377574.6:c.878A>T
MANE Select
|
ENSP00000366797.1:p.Asp293Val
|
|
ENST00000336464.7:c.776A>T
|
ENSP00000336836.7:p.Asp259Val
|
|
ENST00000377567.6:c.554A>T
|
ENSP00000366790.2:p.Asp185Val
|
|
ENST00000377572.5:c.554A>T
|
ENSP00000366795.1:p.Asp185Val
|
|
ENST00000377574.5:c.878A>T
|
ENSP00000366797.1:p.Asp293Val
|
|
ENST00000473690.5:c.215A>T
|
ENSP00000438437.1:p.Asp72Val
|
|
NM_001276326.1:c.776A>T
|
NP_001263255.1:p.Asp259Val
|
|
NM_001276327.1:c.554A>T
|
NP_001263256.1:p.Asp185Val
|
|
NM_144585.3:c.878A>T
|
NP_653186.2:p.Asp293Val
|
|
NM_153378.2:c.215A>T
|
NP_700357.1:p.Asp72Val
|
|
XM_006718430.2:c.953A>T
|
XP_006718493.1:p.Asp318Val
|
|
XM_006718431.2:c.848A>T
|
XP_006718494.1:p.Asp283Val
|
|
XM_006718430.4:c.953A>T
|
XP_006718493.1:p.Asp318Val
|
|
XM_006718431.4:c.848A>T
|
XP_006718494.1:p.Asp283Val
|
|
NM_144585.4:c.878A>T
MANE Select
|
NP_653186.2:p.Asp293Val
|
|
NM_001276326.2:c.776A>T
|
NP_001263255.1:p.Asp259Val
|
|
NM_153378.3:c.215A>T
|
NP_700357.1:p.Asp72Val
|
|
NM_001276327.2:c.554A>T
|
NP_001263256.1:p.Asp185Val
|
|