ENST00000448838.8:c.618T>G
|
ENSP00000389404.3:p.Pro206=
|
|
ENST00000227868.9:c.798T>G
MANE Select
|
ENSP00000227868.4:p.Pro266=
|
|
ENST00000227868.8:c.798T>G
|
ENSP00000227868.4:p.Pro266=
|
|
ENST00000430469.6:c.343-17774T>G
|
ENSP00000415695.2:n.343-17774T>G
|
|
ENST00000448838.7:c.753T>G
|
ENSP00000389404.2:p.Pro251=
|
|
NM_001135024.1:c.753T>G
|
NP_001128496.1:p.Pro251=
|
|
NM_001166158.1:c.343-17774T>G
|
NP_001159630.1:n.343-17774T>G
|
|
NM_003477.2:c.798T>G
|
NP_003468.2:p.Pro266=
|
|
XM_011520390.1:c.618T>G
|
XP_011518692.1:p.Pro206=
|
|
NM_003477.3:c.798T>G
MANE Select
|
NP_003468.2:p.Pro266=
|
|
NM_001135024.2:c.618T>G
|
NP_001128496.2:p.Pro206=
|
|
NM_001166158.2:c.343-17774T>G
|
NP_001159630.1:n.343-17774T>G
|
|