|
ENST00000367698.4:c.1224T=
MANE Select
|
ENSP00000356671.3:p.Asn408=
|
|
|
ENST00000367698.3:c.1224T=
|
ENSP00000356671.3:p.Asn408=
|
|
|
ENST00000617423.4:c.609T=
|
ENSP00000478688.1:p.Asn203=
|
|
|
NM_000488.3:c.1224T= , LRG_577t1:c.1224T=
|
NP_000479.1:p.Asn408=
|
|
|
XM_005245198.2:c.1080T=
|
XP_005245255.1:p.Asn360=
|
|
|
NM_001365052.1:c.1080T=
|
NP_001351981.1:p.Asn360=
|
|
|
NM_000488.4:c.1224T=
MANE Select
|
NP_000479.1:p.Asn408=
|
|
|
NM_001365052.2:c.1080T=
|
NP_001351981.1:p.Asn360=
|
|
|
NM_001386302.1:c.1347T=
|
NP_001373231.1:p.Asn449=
|
|
|
NM_001386303.1:c.1305T=
|
NP_001373232.1:p.Asn435=
|
|
|
NM_001386304.1:c.1203T=
|
NP_001373233.1:p.Asn401=
|
|
|
NM_001386305.1:c.1167T=
|
NP_001373234.1:p.Asn389=
|
|
|
NM_001386306.1:c.1008T=
|
NP_001373235.1:p.Asn336=
|
|
