ENST00000367698.4:c.892G>C
MANE Select
|
ENSP00000356671.3:p.Gly298Arg
|
|
ENST00000367698.3:c.892G>C
|
ENSP00000356671.3:p.Gly298Arg
|
|
ENST00000487183.1:n.543G>C
|
|
|
ENST00000617423.4:c.559+2051G>C
|
ENSP00000478688.1:n.559+2051G>C
|
|
NM_000488.3:c.892G>C , LRG_577t1:c.892G>C
|
NP_000479.1:p.Gly298Arg
|
|
XM_005245198.2:c.748G>C
|
XP_005245255.1:p.Gly250Arg
|
|
NM_001365052.1:c.748G>C
|
NP_001351981.1:p.Gly250Arg
|
|
NM_000488.4:c.892G>C
MANE Select
|
NP_000479.1:p.Gly298Arg
|
|
NM_001365052.2:c.748G>C
|
NP_001351981.1:p.Gly250Arg
|
|
NM_001386302.1:c.1015G>C
|
NP_001373231.1:p.Gly339Arg
|
|
NM_001386303.1:c.973G>C
|
NP_001373232.1:p.Gly325Arg
|
|
NM_001386304.1:c.871G>C
|
NP_001373233.1:p.Gly291Arg
|
|
NM_001386305.1:c.835G>C
|
NP_001373234.1:p.Gly279Arg
|
|
NM_001386306.1:c.676G>C
|
NP_001373235.1:p.Gly226Arg
|
|