ENST00000578493.2:n.1012A>G
|
|
|
ENST00000699291.1:c.804A>G
|
ENSP00000514272.1:n.804A>G
|
|
ENST00000699292.1:n.1214A>G
|
|
|
ENST00000225275.4:c.1679A>G
MANE Select
|
ENSP00000225275.3:p.Gln560Arg
|
|
ENST00000225275.3:c.1679A>G
|
ENSP00000225275.3:p.Gln560Arg
|
|
ENST00000577220.1:c.137A>G
|
ENSP00000464668.1:p.Gln46Arg
|
|
NM_000250.1:c.1679A>G , LRG_84t1:c.1679A>G
|
NP_000241.1:p.Gln560Arg
|
|
XM_011524821.1:c.1865A>G
|
XP_011523123.1:p.Gln622Arg
|
|
XM_011524822.1:c.1394A>G
|
XP_011523124.1:p.Gln465Arg
|
|
NM_000250.2:c.1679A>G
MANE Select
|
NP_000241.1:p.Gln560Arg
|
|