ENST00000320580.9:c.711C>T
MANE Select
|
ENSP00000316454.4:p.Asn237=
|
|
ENST00000320580.8:c.711C>T
|
ENSP00000316454.4:p.Asn237=
|
|
ENST00000527224.1:n.835C>T
|
|
|
ENST00000527380.1:c.417C>T
|
ENSP00000432639.1:p.Asn139=
|
|
NM_018026.3:c.711C>T
|
NP_060496.2:p.Asn237=
|
|
XM_011545162.1:c.390C>T
|
XP_011543464.1:p.Asn130=
|
|
XM_011545163.1:c.381C>T
|
XP_011543465.1:p.Asn127=
|
|
XM_011545164.1:c.372C>T
|
XP_011543466.1:p.Asn124=
|
|
XM_011545164.2:c.372C>T
|
XP_011543466.1:p.Asn124=
|
|
XR_001747924.1:n.922C>T
|
|
|
NM_018026.4:c.711C>T
MANE Select
|
NP_060496.2:p.Asn237=
|
|