ENST00000367698.4:c.936C>T
MANE Select
|
ENSP00000356671.3:p.Thr312=
|
|
ENST00000367698.3:c.936C>T
|
ENSP00000356671.3:p.Thr312=
|
|
ENST00000487183.1:n.587C>T
|
|
|
ENST00000617423.4:c.559+2095C>T
|
ENSP00000478688.1:n.559+2095C>T
|
|
NM_000488.3:c.936C>T , LRG_577t1:c.936C>T
|
NP_000479.1:p.Thr312=
|
|
XM_005245198.2:c.792C>T
|
XP_005245255.1:p.Thr264=
|
|
NM_001365052.1:c.792C>T
|
NP_001351981.1:p.Thr264=
|
|
NM_000488.4:c.936C>T
MANE Select
|
NP_000479.1:p.Thr312=
|
|
NM_001365052.2:c.792C>T
|
NP_001351981.1:p.Thr264=
|
|
NM_001386302.1:c.1059C>T
|
NP_001373231.1:p.Thr353=
|
|
NM_001386303.1:c.1017C>T
|
NP_001373232.1:p.Thr339=
|
|
NM_001386304.1:c.915C>T
|
NP_001373233.1:p.Thr305=
|
|
NM_001386305.1:c.879C>T
|
NP_001373234.1:p.Thr293=
|
|
NM_001386306.1:c.720C>T
|
NP_001373235.1:p.Thr240=
|
|