|
ENST00000367698.4:c.1333A>C
MANE Select
|
ENSP00000356671.3:p.Arg445=
|
|
|
ENST00000367698.3:c.1333A>C
|
ENSP00000356671.3:p.Arg445=
|
|
|
ENST00000617423.4:c.718A>C
|
ENSP00000478688.1:p.Arg240=
|
|
|
NM_000488.3:c.1333A>C , LRG_577t1:c.1333A>C
|
NP_000479.1:p.Arg445=
|
|
|
XM_005245198.2:c.1189A>C
|
XP_005245255.1:p.Arg397=
|
|
|
NM_001365052.1:c.1189A>C
|
NP_001351981.1:p.Arg397=
|
|
|
NM_000488.4:c.1333A>C
MANE Select
|
NP_000479.1:p.Arg445=
|
|
|
NM_001365052.2:c.1189A>C
|
NP_001351981.1:p.Arg397=
|
|
|
NM_001386302.1:c.1456A>C
|
NP_001373231.1:p.Arg486=
|
|
|
NM_001386303.1:c.1414A>C
|
NP_001373232.1:p.Arg472=
|
|
|
NM_001386304.1:c.1312A>C
|
NP_001373233.1:p.Arg438=
|
|
|
NM_001386305.1:c.1276A>C
|
NP_001373234.1:p.Arg426=
|
|
|
NM_001386306.1:c.1117A>C
|
NP_001373235.1:p.Arg373=
|
|
