ENST00000367698.4:c.1231G>C
MANE Select
|
ENSP00000356671.3:p.Gly411Arg
|
|
ENST00000367698.3:c.1231G>C
|
ENSP00000356671.3:p.Gly411Arg
|
|
ENST00000617423.4:c.616G>C
|
ENSP00000478688.1:p.Gly206Arg
|
|
NM_000488.3:c.1231G>C , LRG_577t1:c.1231G>C
|
NP_000479.1:p.Gly411Arg
|
|
XM_005245198.2:c.1087G>C
|
XP_005245255.1:p.Gly363Arg
|
|
NM_001365052.1:c.1087G>C
|
NP_001351981.1:p.Gly363Arg
|
|
NM_000488.4:c.1231G>C
MANE Select
|
NP_000479.1:p.Gly411Arg
|
|
NM_001365052.2:c.1087G>C
|
NP_001351981.1:p.Gly363Arg
|
|
NM_001386302.1:c.1354G>C
|
NP_001373231.1:p.Gly452Arg
|
|
NM_001386303.1:c.1312G>C
|
NP_001373232.1:p.Gly438Arg
|
|
NM_001386304.1:c.1210G>C
|
NP_001373233.1:p.Gly404Arg
|
|
NM_001386305.1:c.1174G>C
|
NP_001373234.1:p.Gly392Arg
|
|
NM_001386306.1:c.1015G>C
|
NP_001373235.1:p.Gly339Arg
|
|