ENST00000578493.2:n.1014A>C
|
|
|
ENST00000699291.1:c.806A>C
|
ENSP00000514272.1:n.806A>C
|
|
ENST00000699292.1:n.1216A>C
|
|
|
ENST00000225275.4:c.1681A>C
MANE Select
|
ENSP00000225275.3:p.Asn561His
|
|
ENST00000225275.3:c.1681A>C
|
ENSP00000225275.3:p.Asn561His
|
|
ENST00000577220.1:c.139A>C
|
ENSP00000464668.1:p.Asn47His
|
|
NM_000250.1:c.1681A>C , LRG_84t1:c.1681A>C
|
NP_000241.1:p.Asn561His
|
|
XM_011524821.1:c.1867A>C
|
XP_011523123.1:p.Asn623His
|
|
XM_011524822.1:c.1396A>C
|
XP_011523124.1:p.Asn466His
|
|
NM_000250.2:c.1681A>C
MANE Select
|
NP_000241.1:p.Asn561His
|
|