|
ENST00000367698.4:c.1240G=
MANE Select
|
ENSP00000356671.3:p.Ala414=
|
|
|
ENST00000367698.3:c.1240G=
|
ENSP00000356671.3:p.Ala414=
|
|
|
ENST00000617423.4:c.625G=
|
ENSP00000478688.1:p.Ala209=
|
|
|
NM_000488.3:c.1240G= , LRG_577t1:c.1240G=
|
NP_000479.1:p.Ala414=
|
|
|
XM_005245198.2:c.1096G=
|
XP_005245255.1:p.Ala366=
|
|
|
NM_001365052.1:c.1096G=
|
NP_001351981.1:p.Ala366=
|
|
|
NM_000488.4:c.1240G=
MANE Select
|
NP_000479.1:p.Ala414=
|
|
|
NM_001365052.2:c.1096G=
|
NP_001351981.1:p.Ala366=
|
|
|
NM_001386302.1:c.1363G=
|
NP_001373231.1:p.Ala455=
|
|
|
NM_001386303.1:c.1321G=
|
NP_001373232.1:p.Ala441=
|
|
|
NM_001386304.1:c.1219G=
|
NP_001373233.1:p.Ala407=
|
|
|
NM_001386305.1:c.1183G=
|
NP_001373234.1:p.Ala395=
|
|
|
NM_001386306.1:c.1024G=
|
NP_001373235.1:p.Ala342=
|
|
