ENST00000269980.7:c.212A>C
MANE Select
|
ENSP00000269980.2:p.Asn71Thr
|
|
ENST00000269980.6:c.212A>C
|
ENSP00000269980.2:p.Asn71Thr
|
|
ENST00000457836.6:c.146A>C
|
ENSP00000416000.2:p.Asn49Thr
|
|
ENST00000538423.5:n.232A>C
|
|
|
ENST00000540732.3:c.314A>C
|
ENSP00000443246.1:p.Asn105Thr
|
|
ENST00000541315.1:c.19A>C
|
|
|
ENST00000542943.5:c.212A>C
|
ENSP00000440345.1:p.Asn71Thr
|
|
ENST00000595085.5:c.212A>C
|
ENSP00000471150.2:p.Asn71Thr
|
|
ENST00000604424.1:n.454A>C
|
|
|
NM_000709.3:c.212A>C
|
NP_000700.1:p.Asn71Thr
|
|
NM_001164783.1:c.212A>C
|
NP_001158255.1:p.Asn71Thr
|
|
NM_000709.4:c.212A>C
MANE Select
|
NP_000700.1:p.Asn71Thr
|
|
NM_001164783.2:c.212A>C
|
NP_001158255.1:p.Asn71Thr
|
|