ENST00000324662.8:c.1086A>C
|
ENSP00000313419.4:p.Gly362=
|
|
ENST00000538922.8:c.1086A>C
MANE Select
|
ENSP00000437940.2:p.Gly362=
|
|
ENST00000324662.7:c.1086A>C
|
ENSP00000313419.3:p.Gly362=
|
|
ENST00000538922.5:c.1086A>C
|
ENSP00000437940.1:p.Gly362=
|
|
ENST00000565089.5:n.1420A>C
|
|
|
ENST00000567368.1:n.226A>C
|
|
|
ENST00000567541.5:c.1086A>C
|
ENSP00000456201.1:p.Gly362=
|
|
ENST00000611258.4:c.1086A>C
|
ENSP00000481090.1:p.Gly362=
|
|
NM_001178098.1:c.1086A>C
|
NP_001171569.1:p.Gly362=
|
|
NM_001770.5:c.1086A>C , LRG_35t1:c.1086A>C
|
NP_001761.3:p.Gly362=
|
|
XM_006721103.2:c.819A>C
|
XP_006721166.1:p.Gly273=
|
|
XR_950871.1:n.1099A>C
|
|
|
XR_950872.1:n.988A>C
|
|
|
XM_006721103.3:c.819A>C
|
XP_006721166.1:p.Gly273=
|
|
XM_017023893.1:c.819A>C
|
XP_016879382.1:p.Gly273=
|
|
XR_950871.2:n.1082A>C
|
|
|
NM_001178098.2:c.1086A>C
|
NP_001171569.1:p.Gly362=
|
|
NM_001770.6:c.1086A>C
MANE Select
|
NP_001761.3:p.Gly362=
|
|
NM_001385732.1:c.819A>C
|
NP_001372661.1:p.Gly273=
|
|
NR_169755.1:n.1428A>C
|
|
|