ENST00000357578.8:c.1291G>C
MANE Select
|
ENSP00000350191.3:p.Asp431His
|
|
ENST00000479394.2:n.406G>C
|
|
|
ENST00000672352.1:c.910G>C
|
ENSP00000500876.1:p.Asp304His
|
|
ENST00000672652.1:c.1254G>C
|
|
|
ENST00000348925.2:c.1330G>C
|
ENSP00000314649.3:p.Asp444His
|
|
ENST00000357578.7:c.1291G>C
|
ENSP00000350191.3:p.Asp431His
|
|
ENST00000479394.1:n.406G>C
|
|
|
ENST00000491546.5:c.1207G>C
|
ENSP00000417687.1:p.Asp403His
|
|
NM_001080.3:c.1291G>C
MANE Select
|
NP_001071.1:p.Asp431His
|
|
NM_170740.1:c.1330G>C
|
NP_733936.1:p.Asp444His
|
|
NM_001368954.1:c.1147G>C
|
NP_001355883.1:p.Asp383His
|
|