ENST00000367698.4:c.1222A>T
MANE Select
|
ENSP00000356671.3:p.Asn408Tyr
|
|
ENST00000367698.3:c.1222A>T
|
ENSP00000356671.3:p.Asn408Tyr
|
|
ENST00000617423.4:c.607A>T
|
ENSP00000478688.1:p.Asn203Tyr
|
|
NM_000488.3:c.1222A>T , LRG_577t1:c.1222A>T
|
NP_000479.1:p.Asn408Tyr
|
|
XM_005245198.2:c.1078A>T
|
XP_005245255.1:p.Asn360Tyr
|
|
NM_001365052.1:c.1078A>T
|
NP_001351981.1:p.Asn360Tyr
|
|
NM_000488.4:c.1222A>T
MANE Select
|
NP_000479.1:p.Asn408Tyr
|
|
NM_001365052.2:c.1078A>T
|
NP_001351981.1:p.Asn360Tyr
|
|
NM_001386302.1:c.1345A>T
|
NP_001373231.1:p.Asn449Tyr
|
|
NM_001386303.1:c.1303A>T
|
NP_001373232.1:p.Asn435Tyr
|
|
NM_001386304.1:c.1201A>T
|
NP_001373233.1:p.Asn401Tyr
|
|
NM_001386305.1:c.1165A>T
|
NP_001373234.1:p.Asn389Tyr
|
|
NM_001386306.1:c.1006A>T
|
NP_001373235.1:p.Asn336Tyr
|
|