ENST00000367698.4:c.924T=
MANE Select
|
ENSP00000356671.3:p.Gly308=
|
|
ENST00000367698.3:c.924T=
|
ENSP00000356671.3:p.Gly308=
|
|
ENST00000487183.1:n.575T=
|
|
|
ENST00000617423.4:c.559+2083T=
|
ENSP00000478688.1:n.559+2083T=
|
|
NM_000488.3:c.924T= , LRG_577t1:c.924T=
|
NP_000479.1:p.Gly308=
|
|
XM_005245198.2:c.780T=
|
XP_005245255.1:p.Gly260=
|
|
NM_001365052.1:c.780T=
|
NP_001351981.1:p.Gly260=
|
|
NM_000488.4:c.924T=
MANE Select
|
NP_000479.1:p.Gly308=
|
|
NM_001365052.2:c.780T=
|
NP_001351981.1:p.Gly260=
|
|
NM_001386302.1:c.1047T=
|
NP_001373231.1:p.Gly349=
|
|
NM_001386303.1:c.1005T=
|
NP_001373232.1:p.Gly335=
|
|
NM_001386304.1:c.903T=
|
NP_001373233.1:p.Gly301=
|
|
NM_001386305.1:c.867T=
|
NP_001373234.1:p.Gly289=
|
|
NM_001386306.1:c.708T=
|
NP_001373235.1:p.Gly236=
|
|