ENST00000258385.8:c.1202T>G
MANE Select
|
ENSP00000258385.3:p.Phe401Cys
|
|
ENST00000258385.7:c.1202T>G
|
ENSP00000258385.3:p.Phe401Cys
|
|
ENST00000441621.6:c.*384T>G
|
ENSP00000408819.2:n.*384T>G
|
|
ENST00000446616.1:c.*843T>G
|
ENSP00000410801.1:n.*843T>G
|
|
ENST00000543200.5:c.1157T>G
|
ENSP00000438380.1:p.Phe386Cys
|
|
NM_000751.2:c.1202T>G
|
NP_000742.1:p.Phe401Cys
|
|
NM_001256657.1:c.1157T>G
|
NP_001243586.1:p.Phe386Cys
|
|
NM_001311195.1:c.620T>G
|
NP_001298124.1:p.Phe207Cys
|
|
NM_001311196.1:c.899T>G
|
NP_001298125.1:p.Phe300Cys
|
|
NR_046333.1:c.-4294966349T>G
|
|
|
NR_046334.1:c.-4294966070T>G
|
|
|
XM_011510524.1:c.821T>G
|
XP_011508826.1:p.Phe274Cys
|
|
XM_011510524.2:c.821T>G
|
XP_011508826.1:p.Phe274Cys
|
|
NM_000751.3:c.1202T>G
MANE Select
|
NP_000742.1:p.Phe401Cys
|
|
NM_001311195.2:c.620T>G
|
NP_001298124.1:p.Phe207Cys
|
|
NM_001311196.2:c.899T>G
|
NP_001298125.1:p.Phe300Cys
|
|
NM_001256657.2:c.1157T>G
|
NP_001243586.1:p.Phe386Cys
|
|