ENST00000324662.8:c.1473A>T
|
ENSP00000313419.4:p.Glu491Asp
|
|
ENST00000538922.8:c.1473A>T
MANE Select
|
ENSP00000437940.2:p.Glu491Asp
|
|
ENST00000324662.7:c.1473A>T
|
ENSP00000313419.3:p.Glu491Asp
|
|
ENST00000538922.5:c.1473A>T
|
ENSP00000437940.1:p.Glu491Asp
|
|
ENST00000565089.5:n.1907A>T
|
|
|
ENST00000567368.1:n.569+132A>T
|
|
|
ENST00000567541.5:c.1473A>T
|
ENSP00000456201.1:p.Glu491Asp
|
|
ENST00000611258.4:c.*68A>T
|
ENSP00000481090.1:n.*68A>T
|
|
NM_001178098.1:c.1473A>T
|
NP_001171569.1:p.Glu491Asp
|
|
NM_001770.5:c.1473A>T , LRG_35t1:c.1473A>T
|
NP_001761.3:p.Glu491Asp
|
|
XM_006721103.2:c.1206A>T
|
XP_006721166.1:p.Glu402Asp
|
|
XM_006721103.3:c.1206A>T
|
XP_006721166.1:p.Glu402Asp
|
|
XM_017023893.1:c.1206A>T
|
XP_016879382.1:p.Glu402Asp
|
|
NM_001178098.2:c.1473A>T
|
NP_001171569.1:p.Glu491Asp
|
|
NM_001770.6:c.1473A>T
MANE Select
|
NP_001761.3:p.Glu491Asp
|
|
NM_001385732.1:c.1206A>T
|
NP_001372661.1:p.Glu402Asp
|
|
NR_169755.1:n.1815A>T
|
|
|