ENST00000527168.6:n.837G>C
|
|
|
ENST00000529110.2:c.822G>C
|
ENSP00000435349.2:p.Arg274Ser
|
|
ENST00000529957.6:n.796G>C
|
|
|
ENST00000683366.1:c.*470G>C
|
ENSP00000507283.1:n.*470G>C
|
|
ENST00000683887.1:c.786G>C
|
ENSP00000506886.1:p.Arg262Ser
|
|
ENST00000684100.1:n.732G>C
|
|
|
ENST00000684126.1:n.872G>C
|
|
|
ENST00000684688.1:n.1363G>C
|
|
|
ENST00000204679.9:c.738G>C
MANE Select
|
ENSP00000204679.4:p.Arg246Ser
|
|
ENST00000204679.8:c.738G>C
|
ENSP00000204679.4:p.Arg246Ser
|
|
ENST00000527076.1:n.1961G>C
|
|
|
ENST00000527168.5:n.905G>C
|
|
|
ENST00000529957.5:n.837G>C
|
|
|
NM_032520.4:c.738G>C
|
NP_115909.1:p.Arg246Ser
|
|
XM_017023782.1:c.786G>C
|
XP_016879271.1:p.Arg262Ser
|
|
XM_017023783.1:c.378G>C
|
XP_016879272.1:p.Arg126Ser
|
|
NM_032520.5:c.738G>C
MANE Select
|
NP_115909.1:p.Arg246Ser
|
|