|
ENST00000367698.4:c.890A>C
MANE Select
|
ENSP00000356671.3:p.Glu297Ala
|
|
|
ENST00000367698.3:c.890A>C
|
ENSP00000356671.3:p.Glu297Ala
|
|
|
ENST00000487183.1:n.541A>C
|
|
|
|
ENST00000617423.4:c.559+2049A>C
|
ENSP00000478688.1:n.559+2049A>C
|
|
|
NM_000488.3:c.890A>C , LRG_577t1:c.890A>C
|
NP_000479.1:p.Glu297Ala
|
|
|
XM_005245198.2:c.746A>C
|
XP_005245255.1:p.Glu249Ala
|
|
|
NM_001365052.1:c.746A>C
|
NP_001351981.1:p.Glu249Ala
|
|
|
NM_000488.4:c.890A>C
MANE Select
|
NP_000479.1:p.Glu297Ala
|
|
|
NM_001365052.2:c.746A>C
|
NP_001351981.1:p.Glu249Ala
|
|
|
NM_001386302.1:c.1013A>C
|
NP_001373231.1:p.Glu338Ala
|
|
|
NM_001386303.1:c.971A>C
|
NP_001373232.1:p.Glu324Ala
|
|
|
NM_001386304.1:c.869A>C
|
NP_001373233.1:p.Glu290Ala
|
|
|
NM_001386305.1:c.833A>C
|
NP_001373234.1:p.Glu278Ala
|
|
|
NM_001386306.1:c.674A>C
|
NP_001373235.1:p.Glu225Ala
|
|
