ENST00000367698.4:c.1087T>G
MANE Select
|
ENSP00000356671.3:p.Leu363Val
|
|
ENST00000367698.3:c.1087T>G
|
ENSP00000356671.3:p.Leu363Val
|
|
ENST00000617423.4:c.560-2125T>G
|
ENSP00000478688.1:n.560-2125T>G
|
|
NM_000488.3:c.1087T>G , LRG_577t1:c.1087T>G
|
NP_000479.1:p.Leu363Val
|
|
XM_005245198.2:c.943T>G
|
XP_005245255.1:p.Leu315Val
|
|
NM_001365052.1:c.943T>G
|
NP_001351981.1:p.Leu315Val
|
|
NM_000488.4:c.1087T>G
MANE Select
|
NP_000479.1:p.Leu363Val
|
|
NM_001365052.2:c.943T>G
|
NP_001351981.1:p.Leu315Val
|
|
NM_001386302.1:c.1210T>G
|
NP_001373231.1:p.Leu404Val
|
|
NM_001386303.1:c.1168T>G
|
NP_001373232.1:p.Leu390Val
|
|
NM_001386304.1:c.1066T>G
|
NP_001373233.1:p.Leu356Val
|
|
NM_001386305.1:c.1030T>G
|
NP_001373234.1:p.Leu344Val
|
|
NM_001386306.1:c.871T>G
|
NP_001373235.1:p.Leu291Val
|
|