ENST00000370263.9:c.1063C>G
MANE Select
|
ENSP00000359285.4:p.Leu355Val
|
|
ENST00000370263.8:c.1063C>G
|
ENSP00000359285.4:p.Leu355Val
|
|
ENST00000463705.5:n.1711C>G
|
|
|
ENST00000467563.3:n.1133C>G
|
|
|
ENST00000498043.6:c.1087C>G
|
|
|
ENST00000615287.4:c.850C>G
|
ENSP00000483388.1:p.Leu284Val
|
|
ENST00000627000.1:c.*752C>G
|
ENSP00000486914.1:n.*752C>G
|
|
ENST00000630240.1:n.784C>G
|
|
|
NM_000744.6:c.1063C>G
|
NP_000735.1:p.Leu355Val
|
|
NM_001256573.1:c.535C>G
|
NP_001243502.1:p.Leu179Val
|
|
NR_046317.1:n.1319C>G
|
|
|
XM_011528524.1:c.850C>G
|
XP_011526826.1:p.Leu284Val
|
|
XM_017027625.2:c.535C>G
|
XP_016883114.1:p.Leu179Val
|
|
XM_024451822.1:c.535C>G
|
XP_024307590.1:p.Leu179Val
|
|
NM_001256573.2:c.535C>G
|
NP_001243502.1:p.Leu179Val
|
|
NR_046317.2:n.1272C>G
|
|
|
NM_000744.7:c.1063C>G
MANE Select
|
NP_000735.1:p.Leu355Val
|
|