ENST00000270357.10:c.1536T>A
MANE Select
|
ENSP00000270357.4:p.Asn512Lys
|
|
ENST00000270357.8:c.843T>A
|
ENSP00000270357.3:p.Asn281Lys
|
|
ENST00000437406.1:c.110-8T>A
|
ENSP00000403319.1:n.110-8T>A
|
|
ENST00000451363.5:c.177T>A
|
ENSP00000414661.1:p.Asn59Lys
|
|
ENST00000464550.5:n.372T>A
|
|
|
ENST00000471657.1:n.339T>A
|
|
|
ENST00000481757.5:n.2470T>A
|
|
|
ENST00000486058.5:n.1649T>A
|
|
|
ENST00000493398.5:n.682T>A
|
|
|
NM_018226.4:c.1536T>A
|
NP_060696.4:p.Asn512Lys
|
|
XM_005247036.3:c.1511-8T>A
|
XP_005247093.1:n.1511-8T>A
|
|
NM_018226.5:c.1536T>A
|
NP_060696.4:p.Asn512Lys
|
|
XM_005247036.4:c.1511-8T>A
|
XP_005247093.1:n.1511-8T>A
|
|
NM_018226.6:c.1536T>A
MANE Select
|
NP_060696.4:p.Asn512Lys
|
|