ENST00000268125.10:c.573G>T
MANE Select
|
ENSP00000268125.5:p.Glu191Asp
|
|
ENST00000268125.9:c.573G>T
|
ENSP00000268125.5:p.Glu191Asp
|
|
ENST00000567787.1:c.*151G>T
|
ENSP00000457251.1:n.*151G>T
|
|
NM_000326.4:c.573G>T
|
NP_000317.1:p.Glu191Asp
|
|
XM_011521870.1:c.573G>T
|
XP_011520172.1:p.Glu191Asp
|
|
XM_011521871.1:c.498G>T
|
XP_011520173.1:p.Glu166Asp
|
|
XM_011521872.1:c.498G>T
|
XP_011520174.1:p.Glu166Asp
|
|
XM_011521870.2:c.573G>T
|
XP_011520172.1:p.Glu191Asp
|
|
XM_017022460.1:c.600G>T
|
XP_016877949.1:p.Glu200Asp
|
|
NM_000326.5:c.573G>T
MANE Select
|
NP_000317.1:p.Glu191Asp
|
|