ENST00000527168.6:n.314T>G
|
|
|
ENST00000529110.2:c.299T>G
|
ENSP00000435349.2:p.Phe100Cys
|
|
ENST00000529957.6:n.273T>G
|
|
|
ENST00000683366.1:c.179-93T>G
|
ENSP00000507283.1:n.179-93T>G
|
|
ENST00000683887.1:c.263T>G
|
ENSP00000506886.1:p.Phe88Cys
|
|
ENST00000684100.1:n.135T>G
|
|
|
ENST00000684126.1:n.273T>G
|
|
|
ENST00000684688.1:n.840T>G
|
|
|
ENST00000204679.9:c.215T>G
MANE Select
|
ENSP00000204679.4:p.Phe72Cys
|
|
ENST00000204679.8:c.215T>G
|
ENSP00000204679.4:p.Phe72Cys
|
|
ENST00000526820.5:c.*117T>G
|
ENSP00000434413.1:n.*117T>G
|
|
ENST00000527076.1:n.1157T>G
|
|
|
ENST00000527168.5:n.270-93T>G
|
|
|
ENST00000529110.1:c.282T>G
|
|
|
ENST00000529957.5:n.314T>G
|
|
|
NM_032520.4:c.215T>G
|
NP_115909.1:p.Phe72Cys
|
|
XM_017023782.1:c.263T>G
|
XP_016879271.1:p.Phe88Cys
|
|
XM_017023783.1:c.-146T>G
|
XP_016879272.1:n.-146T>G
|
|
NM_032520.5:c.215T>G
MANE Select
|
NP_115909.1:p.Phe72Cys
|
|