|
ENST00000367698.4:c.889G>C
MANE Select
|
ENSP00000356671.3:p.Glu297Gln
|
|
|
ENST00000367698.3:c.889G>C
|
ENSP00000356671.3:p.Glu297Gln
|
|
|
ENST00000487183.1:n.540G>C
|
|
|
|
ENST00000617423.4:c.559+2048G>C
|
ENSP00000478688.1:n.559+2048G>C
|
|
|
NM_000488.3:c.889G>C , LRG_577t1:c.889G>C
|
NP_000479.1:p.Glu297Gln
|
|
|
XM_005245198.2:c.745G>C
|
XP_005245255.1:p.Glu249Gln
|
|
|
NM_001365052.1:c.745G>C
|
NP_001351981.1:p.Glu249Gln
|
|
|
NM_000488.4:c.889G>C
MANE Select
|
NP_000479.1:p.Glu297Gln
|
|
|
NM_001365052.2:c.745G>C
|
NP_001351981.1:p.Glu249Gln
|
|
|
NM_001386302.1:c.1012G>C
|
NP_001373231.1:p.Glu338Gln
|
|
|
NM_001386303.1:c.970G>C
|
NP_001373232.1:p.Glu324Gln
|
|
|
NM_001386304.1:c.868G>C
|
NP_001373233.1:p.Glu290Gln
|
|
|
NM_001386305.1:c.832G>C
|
NP_001373234.1:p.Glu278Gln
|
|
|
NM_001386306.1:c.673G>C
|
NP_001373235.1:p.Glu225Gln
|
|
