|
ENST00000367698.4:c.822T>A
MANE Select
|
ENSP00000356671.3:p.Ala274=
|
|
|
ENST00000367698.3:c.822T>A
|
ENSP00000356671.3:p.Ala274=
|
|
|
ENST00000487183.1:n.473T>A
|
|
|
|
ENST00000617423.4:c.559+1981T>A
|
ENSP00000478688.1:n.559+1981T>A
|
|
|
NM_000488.3:c.822T>A , LRG_577t1:c.822T>A
|
NP_000479.1:p.Ala274=
|
|
|
XM_005245198.2:c.678T>A
|
XP_005245255.1:p.Ala226=
|
|
|
NM_001365052.1:c.678T>A
|
NP_001351981.1:p.Ala226=
|
|
|
NM_000488.4:c.822T>A
MANE Select
|
NP_000479.1:p.Ala274=
|
|
|
NM_001365052.2:c.678T>A
|
NP_001351981.1:p.Ala226=
|
|
|
NM_001386302.1:c.945T>A
|
NP_001373231.1:p.Ala315=
|
|
|
NM_001386303.1:c.903T>A
|
NP_001373232.1:p.Ala301=
|
|
|
NM_001386304.1:c.801T>A
|
NP_001373233.1:p.Ala267=
|
|
|
NM_001386305.1:c.765T>A
|
NP_001373234.1:p.Ala255=
|
|
|
NM_001386306.1:c.606T>A
|
NP_001373235.1:p.Ala202=
|
|
