|
ENST00000367698.4:c.896C>T
MANE Select
|
ENSP00000356671.3:p.Thr299Ile
|
|
|
ENST00000367698.3:c.896C>T
|
ENSP00000356671.3:p.Thr299Ile
|
|
|
ENST00000487183.1:n.547C>T
|
|
|
|
ENST00000617423.4:c.559+2055C>T
|
ENSP00000478688.1:n.559+2055C>T
|
|
|
NM_000488.3:c.896C>T , LRG_577t1:c.896C>T
|
NP_000479.1:p.Thr299Ile
|
|
|
XM_005245198.2:c.752C>T
|
XP_005245255.1:p.Thr251Ile
|
|
|
NM_001365052.1:c.752C>T
|
NP_001351981.1:p.Thr251Ile
|
|
|
NM_000488.4:c.896C>T
MANE Select
|
NP_000479.1:p.Thr299Ile
|
|
|
NM_001365052.2:c.752C>T
|
NP_001351981.1:p.Thr251Ile
|
|
|
NM_001386302.1:c.1019C>T
|
NP_001373231.1:p.Thr340Ile
|
|
|
NM_001386303.1:c.977C>T
|
NP_001373232.1:p.Thr326Ile
|
|
|
NM_001386304.1:c.875C>T
|
NP_001373233.1:p.Thr292Ile
|
|
|
NM_001386305.1:c.839C>T
|
NP_001373234.1:p.Thr280Ile
|
|
|
NM_001386306.1:c.680C>T
|
NP_001373235.1:p.Thr227Ile
|
|
