ENST00000367698.4:c.1240G>T
MANE Select
|
ENSP00000356671.3:p.Ala414Ser
|
|
ENST00000367698.3:c.1240G>T
|
ENSP00000356671.3:p.Ala414Ser
|
|
ENST00000617423.4:c.625G>T
|
ENSP00000478688.1:p.Ala209Ser
|
|
NM_000488.3:c.1240G>T , LRG_577t1:c.1240G>T
|
NP_000479.1:p.Ala414Ser
|
|
XM_005245198.2:c.1096G>T
|
XP_005245255.1:p.Ala366Ser
|
|
NM_001365052.1:c.1096G>T
|
NP_001351981.1:p.Ala366Ser
|
|
NM_000488.4:c.1240G>T
MANE Select
|
NP_000479.1:p.Ala414Ser
|
|
NM_001365052.2:c.1096G>T
|
NP_001351981.1:p.Ala366Ser
|
|
NM_001386302.1:c.1363G>T
|
NP_001373231.1:p.Ala455Ser
|
|
NM_001386303.1:c.1321G>T
|
NP_001373232.1:p.Ala441Ser
|
|
NM_001386304.1:c.1219G>T
|
NP_001373233.1:p.Ala407Ser
|
|
NM_001386305.1:c.1183G>T
|
NP_001373234.1:p.Ala395Ser
|
|
NM_001386306.1:c.1024G>T
|
NP_001373235.1:p.Ala342Ser
|
|