|
ENST00000367698.4:c.872G=
MANE Select
|
ENSP00000356671.3:p.Arg291=
|
|
|
ENST00000367698.3:c.872G=
|
ENSP00000356671.3:p.Arg291=
|
|
|
ENST00000487183.1:n.523G=
|
|
|
|
ENST00000617423.4:c.559+2031G=
|
ENSP00000478688.1:n.559+2031G=
|
|
|
NM_000488.3:c.872G= , LRG_577t1:c.872G=
|
NP_000479.1:p.Arg291=
|
|
|
XM_005245198.2:c.728G=
|
XP_005245255.1:p.Arg243=
|
|
|
NM_001365052.1:c.728G=
|
NP_001351981.1:p.Arg243=
|
|
|
NM_000488.4:c.872G=
MANE Select
|
NP_000479.1:p.Arg291=
|
|
|
NM_001365052.2:c.728G=
|
NP_001351981.1:p.Arg243=
|
|
|
NM_001386302.1:c.995G=
|
NP_001373231.1:p.Arg332=
|
|
|
NM_001386303.1:c.953G=
|
NP_001373232.1:p.Arg318=
|
|
|
NM_001386304.1:c.851G=
|
NP_001373233.1:p.Arg284=
|
|
|
NM_001386305.1:c.815G=
|
NP_001373234.1:p.Arg272=
|
|
|
NM_001386306.1:c.656G=
|
NP_001373235.1:p.Arg219=
|
|
