ENST00000296684.10:c.181A>G
MANE Select
|
ENSP00000296684.5:p.Ile61Val
|
|
ENST00000296684.9:c.181A>G
|
ENSP00000296684.5:p.Ile61Val
|
|
ENST00000502423.5:c.*48A>G
|
ENSP00000422177.1:n.*48A>G
|
|
ENST00000506765.1:c.169A>G
|
ENSP00000424570.1:p.Ile57Val
|
|
ENST00000506974.5:c.353A>G
|
ENSP00000425967.1:p.Tyr118Cys
|
|
ENST00000507026.5:c.*155A>G
|
ENSP00000424993.1:n.*155A>G
|
|
ENST00000509443.1:n.42A>G
|
|
|
NM_002495.2:c.181A>G
|
NP_002486.1:p.Ile61Val
|
|
XM_005248525.3:c.181A>G
|
XP_005248582.1:p.Ile61Val
|
|
XM_011543415.1:c.7A>G
|
XP_011541717.1:p.Ile3Val
|
|
NM_001318051.1:c.181A>G
|
NP_001304980.1:p.Ile61Val
|
|
NM_002495.3:c.181A>G
|
NP_002486.1:p.Ile61Val
|
|
NR_134473.1:n.383A>G
|
|
|
NR_134474.1:n.300A>G
|
|
|
NR_134475.1:n.335A>G
|
|
|
NM_002495.4:c.181A>G
MANE Select
|
NP_002486.1:p.Ile61Val
|
|
NM_001318051.2:c.181A>G
|
NP_001304980.1:p.Ile61Val
|
|
NR_134473.2:n.377A>G
|
|
|
NR_134474.2:n.294A>G
|
|
|
NR_134475.2:n.329A>G
|
|
|