ENST00000367324.8:c.881A>T
MANE Select
|
ENSP00000356293.4:p.Asp294Val
|
|
ENST00000263946.7:c.881A>T
|
ENSP00000263946.3:p.Asp294Val
|
|
ENST00000352845.3:c.881A>T
|
ENSP00000295597.3:p.Asp294Val
|
|
ENST00000367324.7:c.881A>T
|
ENSP00000356293.3:p.Asp294Val
|
|
ENST00000475988.1:n.223A>T
|
|
|
ENST00000622031.4:c.878A>T
|
ENSP00000482213.1:p.Asp293Val
|
|
NM_000299.3:c.881A>T
|
NP_000290.2:p.Asp294Val
|
|
NM_001005337.2:c.881A>T
|
NP_001005337.1:p.Asp294Val
|
|
NM_001005337.3:c.881A>T
MANE Select
|
NP_001005337.1:p.Asp294Val
|
|
NM_000299.4:c.881A>T
|
NP_000290.2:p.Asp294Val
|
|