ENST00000527168.6:n.726G=
|
|
|
ENST00000529110.2:c.711G=
|
ENSP00000435349.2:p.Leu237=
|
|
ENST00000529957.6:n.685G=
|
|
|
ENST00000683366.1:c.*359G=
|
ENSP00000507283.1:n.*359G=
|
|
ENST00000683887.1:c.675G=
|
ENSP00000506886.1:p.Leu225=
|
|
ENST00000684100.1:n.621G=
|
|
|
ENST00000684126.1:n.761G=
|
|
|
ENST00000684688.1:n.1252G=
|
|
|
ENST00000204679.9:c.627G=
MANE Select
|
ENSP00000204679.4:p.Leu209=
|
|
ENST00000204679.8:c.627G=
|
ENSP00000204679.4:p.Leu209=
|
|
ENST00000527076.1:n.1850G=
|
|
|
ENST00000527168.5:n.794G=
|
|
|
ENST00000529957.5:n.726G=
|
|
|
NM_032520.4:c.627G=
|
NP_115909.1:p.Leu209=
|
|
XM_017023782.1:c.675G=
|
XP_016879271.1:p.Leu225=
|
|
XM_017023783.1:c.267G=
|
XP_016879272.1:p.Leu89=
|
|
NM_032520.5:c.627G=
MANE Select
|
NP_115909.1:p.Leu209=
|
|