ENST00000367698.4:c.928G>A
MANE Select
|
ENSP00000356671.3:p.Asp310Asn
|
|
ENST00000367698.3:c.928G>A
|
ENSP00000356671.3:p.Asp310Asn
|
|
ENST00000487183.1:n.579G>A
|
|
|
ENST00000617423.4:c.559+2087G>A
|
ENSP00000478688.1:n.559+2087G>A
|
|
NM_000488.3:c.928G>A , LRG_577t1:c.928G>A
|
NP_000479.1:p.Asp310Asn
|
|
XM_005245198.2:c.784G>A
|
XP_005245255.1:p.Asp262Asn
|
|
NM_001365052.1:c.784G>A
|
NP_001351981.1:p.Asp262Asn
|
|
NM_000488.4:c.928G>A
MANE Select
|
NP_000479.1:p.Asp310Asn
|
|
NM_001365052.2:c.784G>A
|
NP_001351981.1:p.Asp262Asn
|
|
NM_001386302.1:c.1051G>A
|
NP_001373231.1:p.Asp351Asn
|
|
NM_001386303.1:c.1009G>A
|
NP_001373232.1:p.Asp337Asn
|
|
NM_001386304.1:c.907G>A
|
NP_001373233.1:p.Asp303Asn
|
|
NM_001386305.1:c.871G>A
|
NP_001373234.1:p.Asp291Asn
|
|
NM_001386306.1:c.712G>A
|
NP_001373235.1:p.Asp238Asn
|
|