ENST00000367698.4:c.904C>G
MANE Select
|
ENSP00000356671.3:p.Leu302Val
|
|
ENST00000367698.3:c.904C>G
|
ENSP00000356671.3:p.Leu302Val
|
|
ENST00000487183.1:n.555C>G
|
|
|
ENST00000617423.4:c.559+2063C>G
|
ENSP00000478688.1:n.559+2063C>G
|
|
NM_000488.3:c.904C>G , LRG_577t1:c.904C>G
|
NP_000479.1:p.Leu302Val
|
|
XM_005245198.2:c.760C>G
|
XP_005245255.1:p.Leu254Val
|
|
NM_001365052.1:c.760C>G
|
NP_001351981.1:p.Leu254Val
|
|
NM_000488.4:c.904C>G
MANE Select
|
NP_000479.1:p.Leu302Val
|
|
NM_001365052.2:c.760C>G
|
NP_001351981.1:p.Leu254Val
|
|
NM_001386302.1:c.1027C>G
|
NP_001373231.1:p.Leu343Val
|
|
NM_001386303.1:c.985C>G
|
NP_001373232.1:p.Leu329Val
|
|
NM_001386304.1:c.883C>G
|
NP_001373233.1:p.Leu295Val
|
|
NM_001386305.1:c.847C>G
|
NP_001373234.1:p.Leu283Val
|
|
NM_001386306.1:c.688C>G
|
NP_001373235.1:p.Leu230Val
|
|