ENST00000367698.4:c.1029G>A
MANE Select
|
ENSP00000356671.3:p.Leu343=
|
|
ENST00000367698.3:c.1029G>A
|
ENSP00000356671.3:p.Leu343=
|
|
ENST00000617423.4:c.560-2183G>A
|
ENSP00000478688.1:n.560-2183G>A
|
|
NM_000488.3:c.1029G>A , LRG_577t1:c.1029G>A
|
NP_000479.1:p.Leu343=
|
|
XM_005245198.2:c.885G>A
|
XP_005245255.1:p.Leu295=
|
|
NM_001365052.1:c.885G>A
|
NP_001351981.1:p.Leu295=
|
|
NM_000488.4:c.1029G>A
MANE Select
|
NP_000479.1:p.Leu343=
|
|
NM_001365052.2:c.885G>A
|
NP_001351981.1:p.Leu295=
|
|
NM_001386302.1:c.1152G>A
|
NP_001373231.1:p.Leu384=
|
|
NM_001386303.1:c.1110G>A
|
NP_001373232.1:p.Leu370=
|
|
NM_001386304.1:c.1008G>A
|
NP_001373233.1:p.Leu336=
|
|
NM_001386305.1:c.972G>A
|
NP_001373234.1:p.Leu324=
|
|
NM_001386306.1:c.813G>A
|
NP_001373235.1:p.Leu271=
|
|