ENST00000527168.6:n.856T>G
|
|
|
ENST00000529110.2:c.841T>G
|
ENSP00000435349.2:p.Ser281Ala
|
|
ENST00000529957.6:n.815T>G
|
|
|
ENST00000683366.1:c.*489T>G
|
ENSP00000507283.1:n.*489T>G
|
|
ENST00000683887.1:c.805T>G
|
ENSP00000506886.1:p.Ser269Ala
|
|
ENST00000684100.1:n.751T>G
|
|
|
ENST00000684126.1:n.891T>G
|
|
|
ENST00000684688.1:n.1382T>G
|
|
|
ENST00000204679.9:c.757T>G
MANE Select
|
ENSP00000204679.4:p.Ser253Ala
|
|
ENST00000204679.8:c.757T>G
|
ENSP00000204679.4:p.Ser253Ala
|
|
ENST00000527076.1:n.1980T>G
|
|
|
ENST00000527168.5:n.924T>G
|
|
|
ENST00000529957.5:n.856T>G
|
|
|
NM_032520.4:c.757T>G
|
NP_115909.1:p.Ser253Ala
|
|
XM_017023782.1:c.805T>G
|
XP_016879271.1:p.Ser269Ala
|
|
XM_017023783.1:c.397T>G
|
XP_016879272.1:p.Ser133Ala
|
|
NM_032520.5:c.757T>G
MANE Select
|
NP_115909.1:p.Ser253Ala
|
|