|
ENST00000367698.4:c.793A>T
MANE Select
|
ENSP00000356671.3:p.Asn265Tyr
|
|
|
ENST00000367698.3:c.793A>T
|
ENSP00000356671.3:p.Asn265Tyr
|
|
|
ENST00000487183.1:n.444A>T
|
|
|
|
ENST00000617423.4:c.559+1952A>T
|
ENSP00000478688.1:n.559+1952A>T
|
|
|
NM_000488.3:c.793A>T , LRG_577t1:c.793A>T
|
NP_000479.1:p.Asn265Tyr
|
|
|
XM_005245198.2:c.649A>T
|
XP_005245255.1:p.Asn217Tyr
|
|
|
NM_001365052.1:c.649A>T
|
NP_001351981.1:p.Asn217Tyr
|
|
|
NM_000488.4:c.793A>T
MANE Select
|
NP_000479.1:p.Asn265Tyr
|
|
|
NM_001365052.2:c.649A>T
|
NP_001351981.1:p.Asn217Tyr
|
|
|
NM_001386302.1:c.916A>T
|
NP_001373231.1:p.Asn306Tyr
|
|
|
NM_001386303.1:c.874A>T
|
NP_001373232.1:p.Asn292Tyr
|
|
|
NM_001386304.1:c.772A>T
|
NP_001373233.1:p.Asn258Tyr
|
|
|
NM_001386305.1:c.763-27A>T
|
NP_001373234.1:n.763-27A>T
|
|
|
NM_001386306.1:c.577A>T
|
NP_001373235.1:p.Asn193Tyr
|
|
