ENST00000527168.6:n.843T=
|
|
|
ENST00000529110.2:c.828T=
|
ENSP00000435349.2:p.Ala276=
|
|
ENST00000529957.6:n.802T=
|
|
|
ENST00000683366.1:c.*476T=
|
ENSP00000507283.1:n.*476T=
|
|
ENST00000683887.1:c.792T=
|
ENSP00000506886.1:p.Ala264=
|
|
ENST00000684100.1:n.738T=
|
|
|
ENST00000684126.1:n.878T=
|
|
|
ENST00000684688.1:n.1369T=
|
|
|
ENST00000204679.9:c.744T=
MANE Select
|
ENSP00000204679.4:p.Ala248=
|
|
ENST00000204679.8:c.744T=
|
ENSP00000204679.4:p.Ala248=
|
|
ENST00000527076.1:n.1967T=
|
|
|
ENST00000527168.5:n.911T=
|
|
|
ENST00000529957.5:n.843T=
|
|
|
NM_032520.4:c.744T=
|
NP_115909.1:p.Ala248=
|
|
XM_017023782.1:c.792T=
|
XP_016879271.1:p.Ala264=
|
|
XM_017023783.1:c.384T=
|
XP_016879272.1:p.Ala128=
|
|
NM_032520.5:c.744T=
MANE Select
|
NP_115909.1:p.Ala248=
|
|