ENST00000296684.10:c.362T>G
MANE Select
|
ENSP00000296684.5:p.Leu121Ter
|
|
ENST00000296684.9:c.362T>G
|
ENSP00000296684.5:p.Leu121Ter
|
|
ENST00000502423.5:c.*229T>G
|
ENSP00000422177.1:n.*229T>G
|
|
ENST00000506765.1:c.338+12157T>G
|
ENSP00000424570.1:n.338+12157T>G
|
|
ENST00000506974.5:c.*138T>G
|
ENSP00000425967.1:n.*138T>G
|
|
ENST00000507026.5:c.*336T>G
|
ENSP00000424993.1:n.*336T>G
|
|
ENST00000509443.1:n.223T>G
|
|
|
NM_002495.2:c.362T>G
|
NP_002486.1:p.Leu121Ter
|
|
XM_005248525.3:c.350+12157T>G
|
XP_005248582.1:n.350+12157T>G
|
|
XM_011543415.1:c.188T>G
|
XP_011541717.1:p.Leu63Ter
|
|
NM_001318051.1:c.350+12157T>G
|
NP_001304980.1:n.350+12157T>G
|
|
NM_002495.3:c.362T>G
|
NP_002486.1:p.Leu121Ter
|
|
NR_134473.1:n.564T>G
|
|
|
NR_134474.1:n.481T>G
|
|
|
NR_134475.1:n.516T>G
|
|
|
NM_002495.4:c.362T>G
MANE Select
|
NP_002486.1:p.Leu121Ter
|
|
NM_001318051.2:c.350+12157T>G
|
NP_001304980.1:n.350+12157T>G
|
|
NR_134473.2:n.558T>G
|
|
|
NR_134474.2:n.475T>G
|
|
|
NR_134475.2:n.510T>G
|
|
|