ENST00000296684.10:c.190T>G
MANE Select
|
ENSP00000296684.5:p.Leu64Val
|
|
ENST00000296684.9:c.190T>G
|
ENSP00000296684.5:p.Leu64Val
|
|
ENST00000502423.5:c.*57T>G
|
ENSP00000422177.1:n.*57T>G
|
|
ENST00000506765.1:c.178T>G
|
ENSP00000424570.1:p.Leu60Val
|
|
ENST00000506974.5:c.362T>G
|
ENSP00000425967.1:p.Phe121Cys
|
|
ENST00000507026.5:c.*164T>G
|
ENSP00000424993.1:n.*164T>G
|
|
ENST00000509443.1:n.51T>G
|
|
|
NM_002495.2:c.190T>G
|
NP_002486.1:p.Leu64Val
|
|
XM_005248525.3:c.190T>G
|
XP_005248582.1:p.Leu64Val
|
|
XM_011543415.1:c.16T>G
|
XP_011541717.1:p.Leu6Val
|
|
NM_001318051.1:c.190T>G
|
NP_001304980.1:p.Leu64Val
|
|
NM_002495.3:c.190T>G
|
NP_002486.1:p.Leu64Val
|
|
NR_134473.1:n.392T>G
|
|
|
NR_134474.1:n.309T>G
|
|
|
NR_134475.1:n.344T>G
|
|
|
NM_002495.4:c.190T>G
MANE Select
|
NP_002486.1:p.Leu64Val
|
|
NM_001318051.2:c.190T>G
|
NP_001304980.1:p.Leu64Val
|
|
NR_134473.2:n.386T>G
|
|
|
NR_134474.2:n.303T>G
|
|
|
NR_134475.2:n.338T>G
|
|
|