ENST00000324662.8:c.1119C>T
|
ENSP00000313419.4:p.Gly373=
|
|
ENST00000538922.8:c.1119C>T
MANE Select
|
ENSP00000437940.2:p.Gly373=
|
|
ENST00000324662.7:c.1119C>T
|
ENSP00000313419.3:p.Gly373=
|
|
ENST00000538922.5:c.1119C>T
|
ENSP00000437940.1:p.Gly373=
|
|
ENST00000565089.5:n.1453C>T
|
|
|
ENST00000567368.1:n.259C>T
|
|
|
ENST00000567541.5:c.1119C>T
|
ENSP00000456201.1:p.Gly373=
|
|
ENST00000611258.4:c.1119C>T
|
ENSP00000481090.1:p.Gly373=
|
|
NM_001178098.1:c.1119C>T
|
NP_001171569.1:p.Gly373=
|
|
NM_001770.5:c.1119C>T , LRG_35t1:c.1119C>T
|
NP_001761.3:p.Gly373=
|
|
XM_006721103.2:c.852C>T
|
XP_006721166.1:p.Gly284=
|
|
XR_950871.1:n.1132C>T
|
|
|
XR_950872.1:n.1021C>T
|
|
|
XM_006721103.3:c.852C>T
|
XP_006721166.1:p.Gly284=
|
|
XM_017023893.1:c.852C>T
|
XP_016879382.1:p.Gly284=
|
|
XR_950871.2:n.1115C>T
|
|
|
NM_001178098.2:c.1119C>T
|
NP_001171569.1:p.Gly373=
|
|
NM_001770.6:c.1119C>T
MANE Select
|
NP_001761.3:p.Gly373=
|
|
NM_001385732.1:c.852C>T
|
NP_001372661.1:p.Gly284=
|
|
NR_169755.1:n.1461C>T
|
|
|