ENST00000367698.4:c.767T=
MANE Select
|
ENSP00000356671.3:p.Leu256=
|
|
ENST00000367698.3:c.767T=
|
ENSP00000356671.3:p.Leu256=
|
|
ENST00000487183.1:n.418T=
|
|
|
ENST00000617423.4:c.559+1926T=
|
ENSP00000478688.1:n.559+1926T=
|
|
NM_000488.3:c.767T= , LRG_577t1:c.767T=
|
NP_000479.1:p.Leu256=
|
|
XM_005245198.2:c.623T=
|
XP_005245255.1:p.Leu208=
|
|
NM_001365052.1:c.623T=
|
NP_001351981.1:p.Leu208=
|
|
NM_000488.4:c.767T=
MANE Select
|
NP_000479.1:p.Leu256=
|
|
NM_001365052.2:c.623T=
|
NP_001351981.1:p.Leu208=
|
|
NM_001386302.1:c.890T=
|
NP_001373231.1:p.Leu297=
|
|
NM_001386303.1:c.848T=
|
NP_001373232.1:p.Leu283=
|
|
NM_001386304.1:c.746T=
|
NP_001373233.1:p.Leu249=
|
|
NM_001386305.1:c.763-53T=
|
NP_001373234.1:n.763-53T=
|
|
NM_001386306.1:c.551T=
|
NP_001373235.1:p.Leu184=
|
|