ENST00000367698.4:c.984G>T
MANE Select
|
ENSP00000356671.3:p.Glu328Asp
|
|
ENST00000367698.3:c.984G>T
|
ENSP00000356671.3:p.Glu328Asp
|
|
ENST00000617423.4:c.559+2143G>T
|
ENSP00000478688.1:n.559+2143G>T
|
|
NM_000488.3:c.984G>T , LRG_577t1:c.984G>T
|
NP_000479.1:p.Glu328Asp
|
|
XM_005245198.2:c.840G>T
|
XP_005245255.1:p.Glu280Asp
|
|
NM_001365052.1:c.840G>T
|
NP_001351981.1:p.Glu280Asp
|
|
NM_000488.4:c.984G>T
MANE Select
|
NP_000479.1:p.Glu328Asp
|
|
NM_001365052.2:c.840G>T
|
NP_001351981.1:p.Glu280Asp
|
|
NM_001386302.1:c.1107G>T
|
NP_001373231.1:p.Glu369Asp
|
|
NM_001386303.1:c.1065G>T
|
NP_001373232.1:p.Glu355Asp
|
|
NM_001386304.1:c.963G>T
|
NP_001373233.1:p.Glu321Asp
|
|
NM_001386305.1:c.927G>T
|
NP_001373234.1:p.Glu309Asp
|
|
NM_001386306.1:c.768G>T
|
NP_001373235.1:p.Glu256Asp
|
|