ENST00000367698.4:c.845C>A
MANE Select
|
ENSP00000356671.3:p.Ser282Tyr
|
|
ENST00000367698.3:c.845C>A
|
ENSP00000356671.3:p.Ser282Tyr
|
|
ENST00000487183.1:n.496C>A
|
|
|
ENST00000617423.4:c.559+2004C>A
|
ENSP00000478688.1:n.559+2004C>A
|
|
NM_000488.3:c.845C>A , LRG_577t1:c.845C>A
|
NP_000479.1:p.Ser282Tyr
|
|
XM_005245198.2:c.701C>A
|
XP_005245255.1:p.Ser234Tyr
|
|
NM_001365052.1:c.701C>A
|
NP_001351981.1:p.Ser234Tyr
|
|
NM_000488.4:c.845C>A
MANE Select
|
NP_000479.1:p.Ser282Tyr
|
|
NM_001365052.2:c.701C>A
|
NP_001351981.1:p.Ser234Tyr
|
|
NM_001386302.1:c.968C>A
|
NP_001373231.1:p.Ser323Tyr
|
|
NM_001386303.1:c.926C>A
|
NP_001373232.1:p.Ser309Tyr
|
|
NM_001386304.1:c.824C>A
|
NP_001373233.1:p.Ser275Tyr
|
|
NM_001386305.1:c.788C>A
|
NP_001373234.1:p.Ser263Tyr
|
|
NM_001386306.1:c.629C>A
|
NP_001373235.1:p.Ser210Tyr
|
|