ENST00000367698.4:c.1038G=
MANE Select
|
ENSP00000356671.3:p.Met346=
|
|
ENST00000367698.3:c.1038G=
|
ENSP00000356671.3:p.Met346=
|
|
ENST00000617423.4:c.560-2174G=
|
ENSP00000478688.1:n.560-2174G=
|
|
NM_000488.3:c.1038G= , LRG_577t1:c.1038G=
|
NP_000479.1:p.Met346=
|
|
XM_005245198.2:c.894G=
|
XP_005245255.1:p.Met298=
|
|
NM_001365052.1:c.894G=
|
NP_001351981.1:p.Met298=
|
|
NM_000488.4:c.1038G=
MANE Select
|
NP_000479.1:p.Met346=
|
|
NM_001365052.2:c.894G=
|
NP_001351981.1:p.Met298=
|
|
NM_001386302.1:c.1161G=
|
NP_001373231.1:p.Met387=
|
|
NM_001386303.1:c.1119G=
|
NP_001373232.1:p.Met373=
|
|
NM_001386304.1:c.1017G=
|
NP_001373233.1:p.Met339=
|
|
NM_001386305.1:c.981G=
|
NP_001373234.1:p.Met327=
|
|
NM_001386306.1:c.822G=
|
NP_001373235.1:p.Met274=
|
|