|
ENST00000367698.4:c.1101G=
MANE Select
|
ENSP00000356671.3:p.Leu367=
|
|
|
ENST00000367698.3:c.1101G=
|
ENSP00000356671.3:p.Leu367=
|
|
|
ENST00000617423.4:c.560-2111G=
|
ENSP00000478688.1:n.560-2111G=
|
|
|
NM_000488.3:c.1101G= , LRG_577t1:c.1101G=
|
NP_000479.1:p.Leu367=
|
|
|
XM_005245198.2:c.957G=
|
XP_005245255.1:p.Leu319=
|
|
|
NM_001365052.1:c.957G=
|
NP_001351981.1:p.Leu319=
|
|
|
NM_000488.4:c.1101G=
MANE Select
|
NP_000479.1:p.Leu367=
|
|
|
NM_001365052.2:c.957G=
|
NP_001351981.1:p.Leu319=
|
|
|
NM_001386302.1:c.1224G=
|
NP_001373231.1:p.Leu408=
|
|
|
NM_001386303.1:c.1182G=
|
NP_001373232.1:p.Leu394=
|
|
|
NM_001386304.1:c.1080G=
|
NP_001373233.1:p.Leu360=
|
|
|
NM_001386305.1:c.1044G=
|
NP_001373234.1:p.Leu348=
|
|
|
NM_001386306.1:c.885G=
|
NP_001373235.1:p.Leu295=
|
|
