ENST00000389805.9:c.971A>T
MANE Select
|
ENSP00000374455.4:p.Glu324Val
|
|
ENST00000360718.5:c.719A>T
|
ENSP00000353944.5:p.Glu240Val
|
|
ENST00000389805.8:c.971A>T
|
ENSP00000374455.4:p.Glu324Val
|
|
ENST00000510187.5:c.950+361A>T
|
ENSP00000424477.1:n.950+361A>T
|
|
NM_001142298.1:c.719A>T
|
NP_001135770.1:p.Glu240Val
|
|
NM_001142299.1:c.719A>T
|
NP_001135771.1:p.Glu240Val
|
|
NM_003900.4:c.971A>T
|
NP_003891.1:p.Glu324Val
|
|
XM_017010010.1:c.719A>T
|
XP_016865499.1:p.Glu240Val
|
|
NM_003900.5:c.971A>T
MANE Select
|
NP_003891.1:p.Glu324Val
|
|
NM_001142298.2:c.719A>T
|
NP_001135770.1:p.Glu240Val
|
|
NM_001142299.2:c.719A>T
|
NP_001135771.1:p.Glu240Val
|
|