ENST00000367698.4:c.1071T=
MANE Select
|
ENSP00000356671.3:p.Ile357=
|
|
ENST00000367698.3:c.1071T=
|
ENSP00000356671.3:p.Ile357=
|
|
ENST00000617423.4:c.560-2141T=
|
ENSP00000478688.1:n.560-2141T=
|
|
NM_000488.3:c.1071T= , LRG_577t1:c.1071T=
|
NP_000479.1:p.Ile357=
|
|
XM_005245198.2:c.927T=
|
XP_005245255.1:p.Ile309=
|
|
NM_001365052.1:c.927T=
|
NP_001351981.1:p.Ile309=
|
|
NM_000488.4:c.1071T=
MANE Select
|
NP_000479.1:p.Ile357=
|
|
NM_001365052.2:c.927T=
|
NP_001351981.1:p.Ile309=
|
|
NM_001386302.1:c.1194T=
|
NP_001373231.1:p.Ile398=
|
|
NM_001386303.1:c.1152T=
|
NP_001373232.1:p.Ile384=
|
|
NM_001386304.1:c.1050T=
|
NP_001373233.1:p.Ile350=
|
|
NM_001386305.1:c.1014T=
|
NP_001373234.1:p.Ile338=
|
|
NM_001386306.1:c.855T=
|
NP_001373235.1:p.Ile285=
|
|