ENST00000527168.6:n.568T>C
|
|
|
ENST00000529110.2:c.553T>C
|
ENSP00000435349.2:p.Cys185Arg
|
|
ENST00000529957.6:n.527T>C
|
|
|
ENST00000683366.1:c.*201T>C
|
ENSP00000507283.1:n.*201T>C
|
|
ENST00000683887.1:c.517T>C
|
ENSP00000506886.1:p.Cys173Arg
|
|
ENST00000684100.1:n.463T>C
|
|
|
ENST00000684126.1:n.527T>C
|
|
|
ENST00000684688.1:n.1094T>C
|
|
|
ENST00000204679.9:c.469T>C
MANE Select
|
ENSP00000204679.4:p.Cys157Arg
|
|
ENST00000204679.8:c.469T>C
|
ENSP00000204679.4:p.Cys157Arg
|
|
ENST00000527076.1:n.1485T>C
|
|
|
ENST00000527168.5:n.505T>C
|
|
|
ENST00000529110.1:c.536T>C
|
|
|
ENST00000529957.5:n.568T>C
|
|
|
NM_032520.4:c.469T>C
|
NP_115909.1:p.Cys157Arg
|
|
XM_017023782.1:c.517T>C
|
XP_016879271.1:p.Cys173Arg
|
|
XM_017023783.1:c.109T>C
|
XP_016879272.1:p.Cys37Arg
|
|
NM_032520.5:c.469T>C
MANE Select
|
NP_115909.1:p.Cys157Arg
|
|