|
ENST00000367698.4:c.972G=
MANE Select
|
ENSP00000356671.3:p.Leu324=
|
|
|
ENST00000367698.3:c.972G=
|
ENSP00000356671.3:p.Leu324=
|
|
|
ENST00000487183.1:n.623G=
|
|
|
|
ENST00000617423.4:c.559+2131G=
|
ENSP00000478688.1:n.559+2131G=
|
|
|
NM_000488.3:c.972G= , LRG_577t1:c.972G=
|
NP_000479.1:p.Leu324=
|
|
|
XM_005245198.2:c.828G=
|
XP_005245255.1:p.Leu276=
|
|
|
NM_001365052.1:c.828G=
|
NP_001351981.1:p.Leu276=
|
|
|
NM_000488.4:c.972G=
MANE Select
|
NP_000479.1:p.Leu324=
|
|
|
NM_001365052.2:c.828G=
|
NP_001351981.1:p.Leu276=
|
|
|
NM_001386302.1:c.1095G=
|
NP_001373231.1:p.Leu365=
|
|
|
NM_001386303.1:c.1053G=
|
NP_001373232.1:p.Leu351=
|
|
|
NM_001386304.1:c.951G=
|
NP_001373233.1:p.Leu317=
|
|
|
NM_001386305.1:c.915G=
|
NP_001373234.1:p.Leu305=
|
|
|
NM_001386306.1:c.756G=
|
NP_001373235.1:p.Leu252=
|
|
