ENST00000340855.11:c.292G>A
MANE Select
|
ENSP00000339801.6:p.Asp98Asn
|
|
ENST00000651111.1:c.-215-2401G>A
|
ENSP00000498395.1:n.-215-2401G>A
|
|
ENST00000340855.10:c.292G>A
|
ENSP00000339801.6:p.Asp98Asn
|
|
ENST00000370441.8:c.292G>A
|
ENSP00000359470.4:p.Asp98Asn
|
|
ENST00000422081.6:c.-215-2401G>A
|
ENSP00000477056.1:n.-215-2401G>A
|
|
ENST00000427113.2:n.770-1215G>A
|
|
|
ENST00000428056.6:c.292G>A
|
ENSP00000390241.2:p.Asp98Asn
|
|
ENST00000441880.1:n.114-16340G>A
|
|
|
ENST00000464251.5:c.115G>A
|
ENSP00000428980.1:p.Asp39Asn
|
|
ENST00000466323.5:c.292G>A
|
ENSP00000418264.1:p.Asp98Asn
|
|
ENST00000523759.5:n.533-2401G>A
|
|
|
NM_000202.6:c.292G>A
|
NP_000193.1:p.Asp98Asn
|
|
NM_001166550.2:c.22G>A
|
NP_001160022.1:p.Asp8Asn
|
|
NM_006123.4:c.292G>A
|
NP_006114.1:p.Asp98Asn
|
|
NR_104128.1:n.509G>A
|
|
|
NM_000202.7:c.292G>A
|
NP_000193.1:p.Asp98Asn
|
|
NM_001166550.3:c.22G>A
|
NP_001160022.1:p.Asp8Asn
|
|
NM_000202.8:c.292G>A
MANE Select
|
NP_000193.1:p.Asp98Asn
|
|
NM_001166550.4:c.22G>A
|
NP_001160022.1:p.Asp8Asn
|
|
NM_006123.5:c.292G>A
|
NP_006114.1:p.Asp98Asn
|
|
NR_104128.2:n.461G>A
|
|
|