|
ENST00000367698.4:c.1235G=
MANE Select
|
ENSP00000356671.3:p.Ser412=
|
|
|
ENST00000367698.3:c.1235G=
|
ENSP00000356671.3:p.Ser412=
|
|
|
ENST00000617423.4:c.620G=
|
ENSP00000478688.1:p.Ser207=
|
|
|
NM_000488.3:c.1235G= , LRG_577t1:c.1235G=
|
NP_000479.1:p.Ser412=
|
|
|
XM_005245198.2:c.1091G=
|
XP_005245255.1:p.Ser364=
|
|
|
NM_001365052.1:c.1091G=
|
NP_001351981.1:p.Ser364=
|
|
|
NM_000488.4:c.1235G=
MANE Select
|
NP_000479.1:p.Ser412=
|
|
|
NM_001365052.2:c.1091G=
|
NP_001351981.1:p.Ser364=
|
|
|
NM_001386302.1:c.1358G=
|
NP_001373231.1:p.Ser453=
|
|
|
NM_001386303.1:c.1316G=
|
NP_001373232.1:p.Ser439=
|
|
|
NM_001386304.1:c.1214G=
|
NP_001373233.1:p.Ser405=
|
|
|
NM_001386305.1:c.1178G=
|
NP_001373234.1:p.Ser393=
|
|
|
NM_001386306.1:c.1019G=
|
NP_001373235.1:p.Ser340=
|
|
