ENST00000296684.10:c.215T>G
MANE Select
|
ENSP00000296684.5:p.Ile72Arg
|
|
ENST00000296684.9:c.215T>G
|
ENSP00000296684.5:p.Ile72Arg
|
|
ENST00000502423.5:c.*82T>G
|
ENSP00000422177.1:n.*82T>G
|
|
ENST00000506765.1:c.203T>G
|
ENSP00000424570.1:p.Ile68Arg
|
|
ENST00000506974.5:c.387T>G
|
ENSP00000425967.1:p.Tyr129Ter
|
|
ENST00000507026.5:c.*189T>G
|
ENSP00000424993.1:n.*189T>G
|
|
ENST00000509443.1:n.76T>G
|
|
|
NM_002495.2:c.215T>G
|
NP_002486.1:p.Ile72Arg
|
|
XM_005248525.3:c.215T>G
|
XP_005248582.1:p.Ile72Arg
|
|
XM_011543415.1:c.41T>G
|
XP_011541717.1:p.Ile14Arg
|
|
NM_001318051.1:c.215T>G
|
NP_001304980.1:p.Ile72Arg
|
|
NM_002495.3:c.215T>G
|
NP_002486.1:p.Ile72Arg
|
|
NR_134473.1:n.417T>G
|
|
|
NR_134474.1:n.334T>G
|
|
|
NR_134475.1:n.369T>G
|
|
|
NM_002495.4:c.215T>G
MANE Select
|
NP_002486.1:p.Ile72Arg
|
|
NM_001318051.2:c.215T>G
|
NP_001304980.1:p.Ile72Arg
|
|
NR_134473.2:n.411T>G
|
|
|
NR_134474.2:n.328T>G
|
|
|
NR_134475.2:n.363T>G
|
|
|