ENST00000466474.6:c.1362C>G
|
ENSP00000511987.1:p.Ser454=
|
|
ENST00000695525.1:n.1560C>G
|
|
|
ENST00000695526.1:c.1399C>G
|
ENSP00000511988.1:p.Leu467Val
|
|
ENST00000695558.1:c.1474C>G
|
ENSP00000512015.1:p.Leu492Val
|
|
ENST00000703224.1:c.*717C>G
|
ENSP00000515242.1:n.*717C>G
|
|
ENST00000359568.10:c.1474C>G
MANE Select
|
ENSP00000352572.5:p.Leu492Val
|
|
ENST00000359568.9:c.1474C>G
|
ENSP00000352572.5:p.Leu492Val
|
|
ENST00000466474.5:n.713C>G
|
|
|
ENST00000480896.5:n.1743C>G
|
|
|
ENST00000483844.1:n.529C>G
|
|
|
NM_001315529.1:c.1120C>G
|
NP_001302458.1:p.Leu374Val
|
|
NM_006031.5:c.1474C>G
|
NP_006022.3:p.Leu492Val
|
|
XM_005261124.3:c.1474C>G
|
XP_005261181.1:p.Leu492Val
|
|
XM_011529593.1:c.1555C>G
|
XP_011527895.1:p.Leu519Val
|
|
XM_011529594.1:c.1555C>G
|
XP_011527896.1:p.Leu519Val
|
|
XM_005261124.5:c.1474C>G
|
XP_005261181.1:p.Leu492Val
|
|
XM_011529594.3:c.1555C>G
|
XP_011527896.1:p.Leu519Val
|
|
XM_017028362.2:c.1474C>G
|
XP_016883851.1:p.Leu492Val
|
|
XM_017028363.1:c.1120C>G
|
XP_016883852.1:p.Leu374Val
|
|
XM_024452082.1:c.358C>G
|
XP_024307850.1:p.Leu120Val
|
|
XM_024452083.1:c.-747C>G
|
XP_024307851.1:n.-747C>G
|
|
NM_006031.6:c.1474C>G
MANE Select
|
NP_006022.3:p.Leu492Val
|
|
NM_001315529.2:c.1120C>G
|
NP_001302458.1:p.Leu374Val
|
|