ENST00000703162.1:n.158A>T
|
|
|
ENST00000281043.4:c.809A>T
MANE Select
|
ENSP00000281043.3:p.Glu270Val
|
|
ENST00000638417.1:c.176A>T
|
ENSP00000491476.1:p.Glu59Val
|
|
ENST00000281043.3:c.809A>T
|
ENSP00000281043.3:p.Glu270Val
|
|
NM_001293228.1:c.809A>T
|
NP_001280157.1:p.Glu270Val
|
|
NM_001293231.1:c.176A>T
|
NP_001280160.1:p.Glu59Val
|
|
NM_001293233.1:c.*744A>T
|
NP_001280162.1:n.*744A>T
|
|
NM_005378.5:c.809A>T
|
NP_005369.2:p.Glu270Val
|
|
NM_005378.6:c.809A>T
MANE Select
|
NP_005369.2:p.Glu270Val
|
|
NM_001293228.2:c.809A>T
|
NP_001280157.1:p.Glu270Val
|
|
NM_001293231.2:c.176A>T
|
NP_001280160.1:p.Glu59Val
|
|
NM_001293233.2:c.*744A>T
|
NP_001280162.1:n.*744A>T
|
|