ENST00000327892.13:c.975G>T
MANE Select
|
ENSP00000339001.7:p.Glu325Asp
|
|
ENST00000680530.1:n.1837G>T
|
|
|
ENST00000681421.1:n.2041G>T
|
|
|
ENST00000681435.1:c.759G>T
|
ENSP00000506665.1:p.Glu253Asp
|
|
ENST00000327892.12:c.975G>T
|
ENSP00000339001.7:p.Glu325Asp
|
|
ENST00000330914.7:c.759G>T
|
ENSP00000365578.2:p.Glu253Asp
|
|
ENST00000396384.1:c.759G>T
|
ENSP00000379668.1:p.Glu253Asp
|
|
ENST00000396389.5:c.921G>T
|
ENSP00000379672.1:p.Glu307Asp
|
|
NM_001293212.1:c.1035G>T
|
NP_001280141.1:p.Glu345Asp
|
|
NM_001293213.1:c.370-1G>T
|
NP_001280142.1:n.370-1G>T
|
|
NM_001293214.1:c.843G>T
|
NP_001280143.1:p.Glu281Asp
|
|
NM_001293215.1:c.759G>T
|
NP_001280144.1:p.Glu253Asp
|
|
NM_001293216.1:c.759G>T
|
NP_001280145.1:p.Glu253Asp
|
|
NM_178014.3:c.975G>T
|
NP_821133.1:p.Glu325Asp
|
|
NR_120608.1:n.682G>T
|
|
|
NM_178014.4:c.975G>T
MANE Select
|
NP_821133.1:p.Glu325Asp
|
|
NM_001293212.2:c.1035G>T
|
NP_001280141.1:p.Glu345Asp
|
|
NM_001293213.2:c.370-1G>T
|
NP_001280142.1:n.370-1G>T
|
|
NM_001293214.2:c.843G>T
|
NP_001280143.1:p.Glu281Asp
|
|
NM_001293215.2:c.759G>T
|
NP_001280144.1:p.Glu253Asp
|
|
NM_001293216.2:c.759G>T
|
NP_001280145.1:p.Glu253Asp
|
|
NR_120608.2:n.531G>T
|
|
|