ENST00000367698.4:c.1275T>G
MANE Select
|
ENSP00000356671.3:p.Arg425=
|
|
ENST00000367698.3:c.1275T>G
|
ENSP00000356671.3:p.Arg425=
|
|
ENST00000617423.4:c.660T>G
|
ENSP00000478688.1:p.Arg220=
|
|
NM_000488.3:c.1275T>G , LRG_577t1:c.1275T>G
|
NP_000479.1:p.Arg425=
|
|
XM_005245198.2:c.1131T>G
|
XP_005245255.1:p.Arg377=
|
|
NM_001365052.1:c.1131T>G
|
NP_001351981.1:p.Arg377=
|
|
NM_000488.4:c.1275T>G
MANE Select
|
NP_000479.1:p.Arg425=
|
|
NM_001365052.2:c.1131T>G
|
NP_001351981.1:p.Arg377=
|
|
NM_001386302.1:c.1398T>G
|
NP_001373231.1:p.Arg466=
|
|
NM_001386303.1:c.1356T>G
|
NP_001373232.1:p.Arg452=
|
|
NM_001386304.1:c.1254T>G
|
NP_001373233.1:p.Arg418=
|
|
NM_001386305.1:c.1218T>G
|
NP_001373234.1:p.Arg406=
|
|
NM_001386306.1:c.1059T>G
|
NP_001373235.1:p.Arg353=
|
|