ENST00000367698.4:c.1295T>G
MANE Select
|
ENSP00000356671.3:p.Val432Gly
|
|
ENST00000367698.3:c.1295T>G
|
ENSP00000356671.3:p.Val432Gly
|
|
ENST00000617423.4:c.680T>G
|
ENSP00000478688.1:p.Val227Gly
|
|
NM_000488.3:c.1295T>G , LRG_577t1:c.1295T>G
|
NP_000479.1:p.Val432Gly
|
|
XM_005245198.2:c.1151T>G
|
XP_005245255.1:p.Val384Gly
|
|
NM_001365052.1:c.1151T>G
|
NP_001351981.1:p.Val384Gly
|
|
NM_000488.4:c.1295T>G
MANE Select
|
NP_000479.1:p.Val432Gly
|
|
NM_001365052.2:c.1151T>G
|
NP_001351981.1:p.Val384Gly
|
|
NM_001386302.1:c.1418T>G
|
NP_001373231.1:p.Val473Gly
|
|
NM_001386303.1:c.1376T>G
|
NP_001373232.1:p.Val459Gly
|
|
NM_001386304.1:c.1274T>G
|
NP_001373233.1:p.Val425Gly
|
|
NM_001386305.1:c.1238T>G
|
NP_001373234.1:p.Val413Gly
|
|
NM_001386306.1:c.1079T>G
|
NP_001373235.1:p.Val360Gly
|
|