ENST00000357578.8:c.1279A>C
MANE Select
|
ENSP00000350191.3:p.Asn427His
|
|
ENST00000479394.2:n.394A>C
|
|
|
ENST00000672352.1:c.898A>C
|
ENSP00000500876.1:p.Asn300His
|
|
ENST00000672652.1:c.1242A>C
|
|
|
ENST00000348925.2:c.1318A>C
|
ENSP00000314649.3:p.Asn440His
|
|
ENST00000357578.7:c.1279A>C
|
ENSP00000350191.3:p.Asn427His
|
|
ENST00000479394.1:n.394A>C
|
|
|
ENST00000491546.5:c.1195A>C
|
ENSP00000417687.1:p.Asn399His
|
|
NM_001080.3:c.1279A>C
MANE Select
|
NP_001071.1:p.Asn427His
|
|
NM_170740.1:c.1318A>C
|
NP_733936.1:p.Asn440His
|
|
NM_001368954.1:c.1135A>C
|
NP_001355883.1:p.Asn379His
|
|