ENST00000578493.2:n.781A>C
|
|
|
ENST00000699291.1:c.573A>C
|
ENSP00000514272.1:p.Gln191His
|
|
ENST00000699292.1:n.488A>C
|
|
|
ENST00000225275.4:c.1448A>C
MANE Select
|
ENSP00000225275.3:p.Asn483Thr
|
|
ENST00000225275.3:c.1448A>C
|
ENSP00000225275.3:p.Asn483Thr
|
|
NM_000250.1:c.1448A>C , LRG_84t1:c.1448A>C
|
NP_000241.1:p.Asn483Thr
|
|
XM_011524821.1:c.1634A>C
|
XP_011523123.1:p.Asn545Thr
|
|
XM_011524822.1:c.1163A>C
|
XP_011523124.1:p.Asn388Thr
|
|
XM_011524823.1:c.1473A>C
|
XP_011523125.1:p.Gln491His
|
|
NM_000250.2:c.1448A>C
MANE Select
|
NP_000241.1:p.Asn483Thr
|
|