ENST00000366930.9:c.1025A>C
MANE Select
|
ENSP00000355897.4:p.Asn342Thr
|
|
ENST00000366929.4:c.1109A>C
|
ENSP00000355896.4:p.Asn370Thr
|
|
ENST00000366930.8:c.1025A>C
|
ENSP00000355897.4:p.Asn342Thr
|
|
ENST00000479322.1:n.509A>C
|
|
|
NM_001135599.2:c.1109A>C
|
NP_001129071.1:p.Asn370Thr
|
|
NM_003238.3:c.1025A>C
|
NP_003229.1:p.Asn342Thr
|
|
NM_001135599.3:c.1109A>C
|
NP_001129071.1:p.Asn370Thr
|
|
NM_003238.4:c.1025A>C
|
NP_003229.1:p.Asn342Thr
|
|
NR_138148.1:n.2328A>C
|
|
|
NR_138149.1:n.2412A>C
|
|
|
NM_003238.5:c.1025A>C
|
NP_003229.1:p.Asn342Thr
|
|
NM_003238.6:c.1025A>C
MANE Select
|
NP_003229.1:p.Asn342Thr
|
|
NM_001135599.4:c.1109A>C
|
NP_001129071.1:p.Asn370Thr
|
|
NR_138148.2:n.2276A>C
|
|
|
NR_138149.2:n.2360A>C
|
|
|