|
ENST00000367698.4:c.1282A>T
MANE Select
|
ENSP00000356671.3:p.Asn428Tyr
|
|
|
ENST00000367698.3:c.1282A>T
|
ENSP00000356671.3:p.Asn428Tyr
|
|
|
ENST00000617423.4:c.667A>T
|
ENSP00000478688.1:p.Asn223Tyr
|
|
|
NM_000488.3:c.1282A>T , LRG_577t1:c.1282A>T
|
NP_000479.1:p.Asn428Tyr
|
|
|
XM_005245198.2:c.1138A>T
|
XP_005245255.1:p.Asn380Tyr
|
|
|
NM_001365052.1:c.1138A>T
|
NP_001351981.1:p.Asn380Tyr
|
|
|
NM_000488.4:c.1282A>T
MANE Select
|
NP_000479.1:p.Asn428Tyr
|
|
|
NM_001365052.2:c.1138A>T
|
NP_001351981.1:p.Asn380Tyr
|
|
|
NM_001386302.1:c.1405A>T
|
NP_001373231.1:p.Asn469Tyr
|
|
|
NM_001386303.1:c.1363A>T
|
NP_001373232.1:p.Asn455Tyr
|
|
|
NM_001386304.1:c.1261A>T
|
NP_001373233.1:p.Asn421Tyr
|
|
|
NM_001386305.1:c.1225A>T
|
NP_001373234.1:p.Asn409Tyr
|
|
|
NM_001386306.1:c.1066A>T
|
NP_001373235.1:p.Asn356Tyr
|
|
