ENST00000366930.9:c.1021T>G
MANE Select
|
ENSP00000355897.4:p.Tyr341Asp
|
|
ENST00000366929.4:c.1105T>G
|
ENSP00000355896.4:p.Tyr369Asp
|
|
ENST00000366930.8:c.1021T>G
|
ENSP00000355897.4:p.Tyr341Asp
|
|
ENST00000479322.1:n.505T>G
|
|
|
NM_001135599.2:c.1105T>G
|
NP_001129071.1:p.Tyr369Asp
|
|
NM_003238.3:c.1021T>G
|
NP_003229.1:p.Tyr341Asp
|
|
NM_001135599.3:c.1105T>G
|
NP_001129071.1:p.Tyr369Asp
|
|
NM_003238.4:c.1021T>G
|
NP_003229.1:p.Tyr341Asp
|
|
NR_138148.1:n.2324T>G
|
|
|
NR_138149.1:n.2408T>G
|
|
|
NM_003238.5:c.1021T>G
|
NP_003229.1:p.Tyr341Asp
|
|
NM_003238.6:c.1021T>G
MANE Select
|
NP_003229.1:p.Tyr341Asp
|
|
NM_001135599.4:c.1105T>G
|
NP_001129071.1:p.Tyr369Asp
|
|
NR_138148.2:n.2272T>G
|
|
|
NR_138149.2:n.2356T>G
|
|
|