ENST00000699289.1:c.37-18754G>A
|
ENSP00000514270.1:n.37-18754G>A
|
|
ENST00000699290.1:c.37-18754G>A
|
ENSP00000514271.1:n.37-18754G>A
|
|
ENST00000374720.8:c.37-18754G>A
MANE Select
|
ENSP00000363852.3:n.37-18754G>A
|
|
ENST00000374720.7:c.37-18754G>A
|
ENSP00000363852.3:n.37-18754G>A
|
|
ENST00000374723.5:c.37-18754G>A
|
ENSP00000363855.1:n.37-18754G>A
|
|
ENST00000374724.1:c.37-18754G>A
|
ENSP00000363856.1:n.37-18754G>A
|
|
ENST00000470972.5:c.37-18754G>A
|
ENSP00000433072.1:n.37-18754G>A
|
|
NM_001286730.1:c.37-18754G>A
|
NP_001273659.1:n.37-18754G>A
|
|
NM_080546.4:c.37-18754G>A
|
NP_536856.2:n.37-18754G>A
|
|
XM_005251855.3:c.37-18754G>A
|
XP_005251912.1:n.37-18754G>A
|
|
XM_006717027.2:c.90+6833G>A
|
XP_006717090.1:n.90+6833G>A
|
|
XM_006717028.2:c.90+6833G>A
|
XP_006717091.1:n.90+6833G>A
|
|
XM_006717029.2:c.90+6833G>A
|
XP_006717092.1:n.90+6833G>A
|
|
NM_001330731.1:c.37-18754G>A
|
NP_001317660.1:n.37-18754G>A
|
|
XM_005251855.4:c.37-18754G>A
|
XP_005251912.1:n.37-18754G>A
|
|
XM_006717027.3:c.90+6833G>A
|
XP_006717090.1:n.90+6833G>A
|
|
XM_006717028.3:c.90+6833G>A
|
XP_006717091.1:n.90+6833G>A
|
|
XM_006717029.3:c.90+6833G>A
|
XP_006717092.1:n.90+6833G>A
|
|
XM_017014560.2:c.-258-18754G>A
|
XP_016870049.1:n.-258-18754G>A
|
|
NM_080546.5:c.37-18754G>A
MANE Select
|
NP_536856.2:n.37-18754G>A
|
|
NM_001286730.2:c.37-18754G>A
|
NP_001273659.1:n.37-18754G>A
|
|
NM_001330731.2:c.37-18754G>A
|
NP_001317660.1:n.37-18754G>A
|
|