ENST00000324662.8:c.1349A>T
|
ENSP00000313419.4:p.Glu450Val
|
|
ENST00000538922.8:c.1349A>T
MANE Select
|
ENSP00000437940.2:p.Glu450Val
|
|
ENST00000324662.7:c.1349A>T
|
ENSP00000313419.3:p.Glu450Val
|
|
ENST00000538922.5:c.1349A>T
|
ENSP00000437940.1:p.Glu450Val
|
|
ENST00000565089.5:n.1683A>T
|
|
|
ENST00000567368.1:n.489A>T
|
|
|
ENST00000567541.5:c.1349A>T
|
ENSP00000456201.1:p.Glu450Val
|
|
ENST00000611258.4:c.1348A>T
|
ENSP00000481090.1:p.Arg450Trp
|
|
NM_001178098.1:c.1349A>T
|
NP_001171569.1:p.Glu450Val
|
|
NM_001770.5:c.1349A>T , LRG_35t1:c.1349A>T
|
NP_001761.3:p.Glu450Val
|
|
XM_006721103.2:c.1082A>T
|
XP_006721166.1:p.Glu361Val
|
|
XM_006721103.3:c.1082A>T
|
XP_006721166.1:p.Glu361Val
|
|
XM_017023893.1:c.1082A>T
|
XP_016879382.1:p.Glu361Val
|
|
NM_001178098.2:c.1349A>T
|
NP_001171569.1:p.Glu450Val
|
|
NM_001770.6:c.1349A>T
MANE Select
|
NP_001761.3:p.Glu450Val
|
|
NM_001385732.1:c.1082A>T
|
NP_001372661.1:p.Glu361Val
|
|
NR_169755.1:n.1691A>T
|
|
|