ENST00000366930.9:c.943G>T
MANE Select
|
ENSP00000355897.4:p.Asp315Tyr
|
|
ENST00000366929.4:c.1027G>T
|
ENSP00000355896.4:p.Asp343Tyr
|
|
ENST00000366930.8:c.943G>T
|
ENSP00000355897.4:p.Asp315Tyr
|
|
ENST00000479322.1:n.427G>T
|
|
|
NM_001135599.2:c.1027G>T
|
NP_001129071.1:p.Asp343Tyr
|
|
NM_003238.3:c.943G>T
|
NP_003229.1:p.Asp315Tyr
|
|
NM_001135599.3:c.1027G>T
|
NP_001129071.1:p.Asp343Tyr
|
|
NM_003238.4:c.943G>T
|
NP_003229.1:p.Asp315Tyr
|
|
NR_138148.1:n.2246G>T
|
|
|
NR_138149.1:n.2330G>T
|
|
|
NM_003238.5:c.943G>T
|
NP_003229.1:p.Asp315Tyr
|
|
NM_003238.6:c.943G>T
MANE Select
|
NP_003229.1:p.Asp315Tyr
|
|
NM_001135599.4:c.1027G>T
|
NP_001129071.1:p.Asp343Tyr
|
|
NR_138148.2:n.2194G>T
|
|
|
NR_138149.2:n.2278G>T
|
|
|