ENST00000389805.9:c.1154A>G
MANE Select
|
ENSP00000374455.4:p.His385Arg
|
|
ENST00000360718.5:c.902A>G
|
ENSP00000353944.5:p.His301Arg
|
|
ENST00000389805.8:c.1154A>G
|
ENSP00000374455.4:p.His385Arg
|
|
ENST00000510187.5:c.950+544A>G
|
ENSP00000424477.1:n.950+544A>G
|
|
NM_001142298.1:c.902A>G
|
NP_001135770.1:p.His301Arg
|
|
NM_001142299.1:c.902A>G
|
NP_001135771.1:p.His301Arg
|
|
NM_003900.4:c.1154A>G
|
NP_003891.1:p.His385Arg
|
|
XM_017010010.1:c.902A>G
|
XP_016865499.1:p.His301Arg
|
|
NM_003900.5:c.1154A>G
MANE Select
|
NP_003891.1:p.His385Arg
|
|
NM_001142298.2:c.902A>G
|
NP_001135770.1:p.His301Arg
|
|
NM_001142299.2:c.902A>G
|
NP_001135771.1:p.His301Arg
|
|