ENST00000367698.4:c.1233C>G
MANE Select
|
ENSP00000356671.3:p.Gly411=
|
|
ENST00000367698.3:c.1233C>G
|
ENSP00000356671.3:p.Gly411=
|
|
ENST00000617423.4:c.618C>G
|
ENSP00000478688.1:p.Gly206=
|
|
NM_000488.3:c.1233C>G , LRG_577t1:c.1233C>G
|
NP_000479.1:p.Gly411=
|
|
XM_005245198.2:c.1089C>G
|
XP_005245255.1:p.Gly363=
|
|
NM_001365052.1:c.1089C>G
|
NP_001351981.1:p.Gly363=
|
|
NM_000488.4:c.1233C>G
MANE Select
|
NP_000479.1:p.Gly411=
|
|
NM_001365052.2:c.1089C>G
|
NP_001351981.1:p.Gly363=
|
|
NM_001386302.1:c.1356C>G
|
NP_001373231.1:p.Gly452=
|
|
NM_001386303.1:c.1314C>G
|
NP_001373232.1:p.Gly438=
|
|
NM_001386304.1:c.1212C>G
|
NP_001373233.1:p.Gly404=
|
|
NM_001386305.1:c.1176C>G
|
NP_001373234.1:p.Gly392=
|
|
NM_001386306.1:c.1017C>G
|
NP_001373235.1:p.Gly339=
|
|