ENST00000315491.12:c.893A>C
MANE Select
|
ENSP00000320295.7:p.Asn298Thr
|
|
ENST00000680788.1:n.4314A>C
|
|
|
ENST00000315491.11:c.893A>C
|
ENSP00000320295.7:p.Asn298Thr
|
|
ENST00000554444.5:c.677A>C
|
ENSP00000451617.1:p.Asn226Thr
|
|
ENST00000555576.5:c.277+1766A>C
|
ENSP00000452554.1:n.277+1766A>C
|
|
ENST00000555609.5:c.*978A>C
|
ENSP00000451276.1:n.*978A>C
|
|
ENST00000556922.1:c.1934A>C
|
ENSP00000451560.1:p.Asn645Thr
|
|
NM_001197181.1:c.677A>C
|
NP_001184110.1:p.Asn226Thr
|
|
NM_006086.3:c.893A>C
|
NP_006077.2:p.Asn298Thr
|
|
NM_006086.4:c.893A>C
MANE Select
|
NP_006077.2:p.Asn298Thr
|
|
NM_001197181.2:c.677A>C
|
NP_001184110.1:p.Asn226Thr
|
|