|
ENST00000367698.4:c.1278G>T
MANE Select
|
ENSP00000356671.3:p.Ser426=
|
|
|
ENST00000367698.3:c.1278G>T
|
ENSP00000356671.3:p.Ser426=
|
|
|
ENST00000617423.4:c.663G>T
|
ENSP00000478688.1:p.Ser221=
|
|
|
NM_000488.3:c.1278G>T , LRG_577t1:c.1278G>T
|
NP_000479.1:p.Ser426=
|
|
|
XM_005245198.2:c.1134G>T
|
XP_005245255.1:p.Ser378=
|
|
|
NM_001365052.1:c.1134G>T
|
NP_001351981.1:p.Ser378=
|
|
|
NM_000488.4:c.1278G>T
MANE Select
|
NP_000479.1:p.Ser426=
|
|
|
NM_001365052.2:c.1134G>T
|
NP_001351981.1:p.Ser378=
|
|
|
NM_001386302.1:c.1401G>T
|
NP_001373231.1:p.Ser467=
|
|
|
NM_001386303.1:c.1359G>T
|
NP_001373232.1:p.Ser453=
|
|
|
NM_001386304.1:c.1257G>T
|
NP_001373233.1:p.Ser419=
|
|
|
NM_001386305.1:c.1221G>T
|
NP_001373234.1:p.Ser407=
|
|
|
NM_001386306.1:c.1062G>T
|
NP_001373235.1:p.Ser354=
|
|
