ENST00000389805.9:c.1165+116T>A
MANE Select
|
ENSP00000374455.4:n.1165+116T>A
|
|
ENST00000360718.5:c.913+116T>A
|
ENSP00000353944.5:n.913+116T>A
|
|
ENST00000389805.8:c.1165+116T>A
|
ENSP00000374455.4:n.1165+116T>A
|
|
ENST00000510187.5:c.950+671T>A
|
ENSP00000424477.1:n.950+671T>A
|
|
NM_001142298.1:c.913+116T>A
|
NP_001135770.1:n.913+116T>A
|
|
NM_001142299.1:c.913+116T>A
|
NP_001135771.1:n.913+116T>A
|
|
NM_003900.4:c.1165+116T>A
|
NP_003891.1:n.1165+116T>A
|
|
XM_017010010.1:c.913+116T>A
|
XP_016865499.1:n.913+116T>A
|
|
NM_003900.5:c.1165+116T>A
MANE Select
|
NP_003891.1:n.1165+116T>A
|
|
NM_001142298.2:c.913+116T>A
|
NP_001135770.1:n.913+116T>A
|
|
NM_001142299.2:c.913+116T>A
|
NP_001135771.1:n.913+116T>A
|
|