ENST00000527168.6:n.727A>G
|
|
|
ENST00000529110.2:c.712A>G
|
ENSP00000435349.2:p.Arg238Gly
|
|
ENST00000529957.6:n.686A>G
|
|
|
ENST00000683366.1:c.*360A>G
|
ENSP00000507283.1:n.*360A>G
|
|
ENST00000683887.1:c.676A>G
|
ENSP00000506886.1:p.Arg226Gly
|
|
ENST00000684100.1:n.622A>G
|
|
|
ENST00000684126.1:n.762A>G
|
|
|
ENST00000684688.1:n.1253A>G
|
|
|
ENST00000204679.9:c.628A>G
MANE Select
|
ENSP00000204679.4:p.Arg210Gly
|
|
ENST00000204679.8:c.628A>G
|
ENSP00000204679.4:p.Arg210Gly
|
|
ENST00000527076.1:n.1851A>G
|
|
|
ENST00000527168.5:n.795A>G
|
|
|
ENST00000529957.5:n.727A>G
|
|
|
NM_032520.4:c.628A>G
|
NP_115909.1:p.Arg210Gly
|
|
XM_017023782.1:c.676A>G
|
XP_016879271.1:p.Arg226Gly
|
|
XM_017023783.1:c.268A>G
|
XP_016879272.1:p.Arg90Gly
|
|
NM_032520.5:c.628A>G
MANE Select
|
NP_115909.1:p.Arg210Gly
|
|