ENST00000578493.2:n.793A>T
|
|
|
ENST00000699291.1:c.585A>T
|
ENSP00000514272.1:n.585A>T
|
|
ENST00000699292.1:n.500A>T
|
|
|
ENST00000225275.4:c.1460A>T
MANE Select
|
ENSP00000225275.3:p.Asp487Val
|
|
ENST00000225275.3:c.1460A>T
|
ENSP00000225275.3:p.Asp487Val
|
|
NM_000250.1:c.1460A>T , LRG_84t1:c.1460A>T
|
NP_000241.1:p.Asp487Val
|
|
XM_011524821.1:c.1646A>T
|
XP_011523123.1:p.Asp549Val
|
|
XM_011524822.1:c.1175A>T
|
XP_011523124.1:p.Asp392Val
|
|
XM_011524823.1:c.*9A>T
|
XP_011523125.1:n.*9A>T
|
|
NM_000250.2:c.1460A>T
MANE Select
|
NP_000241.1:p.Asp487Val
|
|