ENST00000578493.2:n.782T>C
|
|
|
ENST00000699291.1:c.574T>C
|
ENSP00000514272.1:p.Ter192Arg
|
|
ENST00000699292.1:n.489T>C
|
|
|
ENST00000225275.4:c.1449T>C
MANE Select
|
ENSP00000225275.3:p.Asn483=
|
|
ENST00000225275.3:c.1449T>C
|
ENSP00000225275.3:p.Asn483=
|
|
NM_000250.1:c.1449T>C , LRG_84t1:c.1449T>C
|
NP_000241.1:p.Asn483=
|
|
XM_011524821.1:c.1635T>C
|
XP_011523123.1:p.Asn545=
|
|
XM_011524822.1:c.1164T>C
|
XP_011523124.1:p.Asn388=
|
|
XM_011524823.1:c.1474T>C
|
XP_011523125.1:p.Ter492Arg
|
|
NM_000250.2:c.1449T>C
MANE Select
|
NP_000241.1:p.Asn483=
|
|