ENST00000367698.4:c.980T>A
MANE Select
|
ENSP00000356671.3:p.Val327Glu
|
|
ENST00000367698.3:c.980T>A
|
ENSP00000356671.3:p.Val327Glu
|
|
ENST00000617423.4:c.559+2139T>A
|
ENSP00000478688.1:n.559+2139T>A
|
|
NM_000488.3:c.980T>A , LRG_577t1:c.980T>A
|
NP_000479.1:p.Val327Glu
|
|
XM_005245198.2:c.836T>A
|
XP_005245255.1:p.Val279Glu
|
|
NM_001365052.1:c.836T>A
|
NP_001351981.1:p.Val279Glu
|
|
NM_000488.4:c.980T>A
MANE Select
|
NP_000479.1:p.Val327Glu
|
|
NM_001365052.2:c.836T>A
|
NP_001351981.1:p.Val279Glu
|
|
NM_001386302.1:c.1103T>A
|
NP_001373231.1:p.Val368Glu
|
|
NM_001386303.1:c.1061T>A
|
NP_001373232.1:p.Val354Glu
|
|
NM_001386304.1:c.959T>A
|
NP_001373233.1:p.Val320Glu
|
|
NM_001386305.1:c.923T>A
|
NP_001373234.1:p.Val308Glu
|
|
NM_001386306.1:c.764T>A
|
NP_001373235.1:p.Val255Glu
|
|