ENST00000367698.4:c.1273C>G
MANE Select
|
ENSP00000356671.3:p.Arg425Gly
|
|
ENST00000367698.3:c.1273C>G
|
ENSP00000356671.3:p.Arg425Gly
|
|
ENST00000617423.4:c.658C>G
|
ENSP00000478688.1:p.Arg220Gly
|
|
NM_000488.3:c.1273C>G , LRG_577t1:c.1273C>G
|
NP_000479.1:p.Arg425Gly
|
|
XM_005245198.2:c.1129C>G
|
XP_005245255.1:p.Arg377Gly
|
|
NM_001365052.1:c.1129C>G
|
NP_001351981.1:p.Arg377Gly
|
|
NM_000488.4:c.1273C>G
MANE Select
|
NP_000479.1:p.Arg425Gly
|
|
NM_001365052.2:c.1129C>G
|
NP_001351981.1:p.Arg377Gly
|
|
NM_001386302.1:c.1396C>G
|
NP_001373231.1:p.Arg466Gly
|
|
NM_001386303.1:c.1354C>G
|
NP_001373232.1:p.Arg452Gly
|
|
NM_001386304.1:c.1252C>G
|
NP_001373233.1:p.Arg418Gly
|
|
NM_001386305.1:c.1216C>G
|
NP_001373234.1:p.Arg406Gly
|
|
NM_001386306.1:c.1057C>G
|
NP_001373235.1:p.Arg353Gly
|
|