ENST00000330062.8:c.407A>C
MANE Select
|
ENSP00000331897.4:p.Asn136Thr
|
|
ENST00000330062.7:c.407A>C
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ENSP00000331897.3:p.Asn136Thr
|
|
ENST00000540499.2:c.251A>C
|
ENSP00000446147.2:p.Asn84Thr
|
|
ENST00000559482.5:c.208-212A>C
|
ENSP00000453016.1:n.208-212A>C
|
|
ENST00000560061.1:c.*32A>C
|
ENSP00000453254.1:n.*32A>C
|
|
NM_001289910.1:c.251A>C , LRG_611t1:c.251A>C
|
NP_001276839.1:p.Asn84Thr
|
|
NM_001290114.1:c.17A>C
|
NP_001277043.1:p.Asn6Thr
|
|
NM_002168.3:c.407A>C , LRG_611t2:c.407A>C
|
NP_002159.2:p.Asn136Thr
|
|
NM_001290114.2:c.17A>C
|
NP_001277043.1:p.Asn6Thr
|
|
NM_002168.4:c.407A>C
MANE Select
|
NP_002159.2:p.Asn136Thr
|
|