|
ENST00000367698.4:c.841G>T
MANE Select
|
ENSP00000356671.3:p.Ala281Ser
|
|
|
ENST00000367698.3:c.841G>T
|
ENSP00000356671.3:p.Ala281Ser
|
|
|
ENST00000487183.1:n.492G>T
|
|
|
|
ENST00000617423.4:c.559+2000G>T
|
ENSP00000478688.1:n.559+2000G>T
|
|
|
NM_000488.3:c.841G>T , LRG_577t1:c.841G>T
|
NP_000479.1:p.Ala281Ser
|
|
|
XM_005245198.2:c.697G>T
|
XP_005245255.1:p.Ala233Ser
|
|
|
NM_001365052.1:c.697G>T
|
NP_001351981.1:p.Ala233Ser
|
|
|
NM_000488.4:c.841G>T
MANE Select
|
NP_000479.1:p.Ala281Ser
|
|
|
NM_001365052.2:c.697G>T
|
NP_001351981.1:p.Ala233Ser
|
|
|
NM_001386302.1:c.964G>T
|
NP_001373231.1:p.Ala322Ser
|
|
|
NM_001386303.1:c.922G>T
|
NP_001373232.1:p.Ala308Ser
|
|
|
NM_001386304.1:c.820G>T
|
NP_001373233.1:p.Ala274Ser
|
|
|
NM_001386305.1:c.784G>T
|
NP_001373234.1:p.Ala262Ser
|
|
|
NM_001386306.1:c.625G>T
|
NP_001373235.1:p.Ala209Ser
|
|
