ENST00000357578.8:c.591G=
MANE Select
|
ENSP00000350191.3:p.Val197=
|
|
ENST00000672352.1:c.354G=
|
ENSP00000500876.1:p.Val118=
|
|
ENST00000672557.1:c.509G=
|
|
|
ENST00000672652.1:c.512G=
|
|
|
ENST00000675422.1:n.1351G=
|
|
|
ENST00000348925.2:c.591G=
|
ENSP00000314649.3:p.Val197=
|
|
ENST00000357578.7:c.591G=
|
ENSP00000350191.3:p.Val197=
|
|
ENST00000491546.5:c.507G=
|
ENSP00000417687.1:p.Val169=
|
|
NM_001080.3:c.591G=
MANE Select
|
NP_001071.1:p.Val197=
|
|
NM_170740.1:c.591G=
|
NP_733936.1:p.Val197=
|
|
NM_001368954.1:c.591G=
|
NP_001355883.1:p.Val197=
|
|