ENST00000367698.4:c.1373T>G
MANE Select
|
ENSP00000356671.3:p.Val458Gly
|
|
ENST00000367698.3:c.1373T>G
|
ENSP00000356671.3:p.Val458Gly
|
|
ENST00000617423.4:c.758T>G
|
ENSP00000478688.1:p.Val253Gly
|
|
NM_000488.3:c.1373T>G , LRG_577t1:c.1373T>G
|
NP_000479.1:p.Val458Gly
|
|
XM_005245198.2:c.1229T>G
|
XP_005245255.1:p.Val410Gly
|
|
NM_001365052.1:c.1229T>G
|
NP_001351981.1:p.Val410Gly
|
|
NM_000488.4:c.1373T>G
MANE Select
|
NP_000479.1:p.Val458Gly
|
|
NM_001365052.2:c.1229T>G
|
NP_001351981.1:p.Val410Gly
|
|
NM_001386302.1:c.1496T>G
|
NP_001373231.1:p.Val499Gly
|
|
NM_001386303.1:c.1454T>G
|
NP_001373232.1:p.Val485Gly
|
|
NM_001386304.1:c.1352T>G
|
NP_001373233.1:p.Val451Gly
|
|
NM_001386305.1:c.1316T>G
|
NP_001373234.1:p.Val439Gly
|
|
NM_001386306.1:c.1157T>G
|
NP_001373235.1:p.Val386Gly
|
|