ENST00000367698.4:c.1070T>A
MANE Select
|
ENSP00000356671.3:p.Ile357Asn
|
|
ENST00000367698.3:c.1070T>A
|
ENSP00000356671.3:p.Ile357Asn
|
|
ENST00000617423.4:c.560-2142T>A
|
ENSP00000478688.1:n.560-2142T>A
|
|
NM_000488.3:c.1070T>A , LRG_577t1:c.1070T>A
|
NP_000479.1:p.Ile357Asn
|
|
XM_005245198.2:c.926T>A
|
XP_005245255.1:p.Ile309Asn
|
|
NM_001365052.1:c.926T>A
|
NP_001351981.1:p.Ile309Asn
|
|
NM_000488.4:c.1070T>A
MANE Select
|
NP_000479.1:p.Ile357Asn
|
|
NM_001365052.2:c.926T>A
|
NP_001351981.1:p.Ile309Asn
|
|
NM_001386302.1:c.1193T>A
|
NP_001373231.1:p.Ile398Asn
|
|
NM_001386303.1:c.1151T>A
|
NP_001373232.1:p.Ile384Asn
|
|
NM_001386304.1:c.1049T>A
|
NP_001373233.1:p.Ile350Asn
|
|
NM_001386305.1:c.1013T>A
|
NP_001373234.1:p.Ile338Asn
|
|
NM_001386306.1:c.854T>A
|
NP_001373235.1:p.Ile285Asn
|
|