|
ENST00000367698.4:c.819G>A
MANE Select
|
ENSP00000356671.3:p.Lys273=
|
|
|
ENST00000367698.3:c.819G>A
|
ENSP00000356671.3:p.Lys273=
|
|
|
ENST00000487183.1:n.470G>A
|
|
|
|
ENST00000617423.4:c.559+1978G>A
|
ENSP00000478688.1:n.559+1978G>A
|
|
|
NM_000488.3:c.819G>A , LRG_577t1:c.819G>A
|
NP_000479.1:p.Lys273=
|
|
|
XM_005245198.2:c.675G>A
|
XP_005245255.1:p.Lys225=
|
|
|
NM_001365052.1:c.675G>A
|
NP_001351981.1:p.Lys225=
|
|
|
NM_000488.4:c.819G>A
MANE Select
|
NP_000479.1:p.Lys273=
|
|
|
NM_001365052.2:c.675G>A
|
NP_001351981.1:p.Lys225=
|
|
|
NM_001386302.1:c.942G>A
|
NP_001373231.1:p.Lys314=
|
|
|
NM_001386303.1:c.900G>A
|
NP_001373232.1:p.Lys300=
|
|
|
NM_001386304.1:c.798G>A
|
NP_001373233.1:p.Lys266=
|
|
|
NM_001386305.1:c.763-1G>A
|
NP_001373234.1:n.763-1G>A
|
|
|
NM_001386306.1:c.603G>A
|
NP_001373235.1:p.Lys201=
|
|
