ENST00000357578.8:c.1301G>T
MANE Select
|
ENSP00000350191.3:p.Cys434Phe
|
|
ENST00000479394.2:n.416G>T
|
|
|
ENST00000672352.1:c.920G>T
|
ENSP00000500876.1:p.Cys307Phe
|
|
ENST00000672652.1:c.1264G>T
|
|
|
ENST00000348925.2:c.1340G>T
|
ENSP00000314649.3:p.Cys447Phe
|
|
ENST00000357578.7:c.1301G>T
|
ENSP00000350191.3:p.Cys434Phe
|
|
ENST00000479394.1:n.416G>T
|
|
|
ENST00000491546.5:c.1217G>T
|
ENSP00000417687.1:p.Cys406Phe
|
|
NM_001080.3:c.1301G>T
MANE Select
|
NP_001071.1:p.Cys434Phe
|
|
NM_170740.1:c.1340G>T
|
NP_733936.1:p.Cys447Phe
|
|
NM_001368954.1:c.1157G>T
|
NP_001355883.1:p.Cys386Phe
|
|