ENST00000527168.6:n.901A>T
|
|
|
ENST00000529110.2:c.886A>T
|
ENSP00000435349.2:p.Ile296Phe
|
|
ENST00000529957.6:n.860A>T
|
|
|
ENST00000683366.1:c.*534A>T
|
ENSP00000507283.1:n.*534A>T
|
|
ENST00000683887.1:c.850A>T
|
ENSP00000506886.1:p.Ile284Phe
|
|
ENST00000684100.1:n.796A>T
|
|
|
ENST00000684126.1:n.936A>T
|
|
|
ENST00000684688.1:n.1427A>T
|
|
|
ENST00000204679.9:c.802A>T
MANE Select
|
ENSP00000204679.4:p.Ile268Phe
|
|
ENST00000204679.8:c.802A>T
|
ENSP00000204679.4:p.Ile268Phe
|
|
ENST00000527076.1:n.2025A>T
|
|
|
ENST00000527168.5:n.969A>T
|
|
|
ENST00000529957.5:n.901A>T
|
|
|
NM_032520.4:c.802A>T
|
NP_115909.1:p.Ile268Phe
|
|
XM_017023782.1:c.850A>T
|
XP_016879271.1:p.Ile284Phe
|
|
XM_017023783.1:c.442A>T
|
XP_016879272.1:p.Ile148Phe
|
|
NM_032520.5:c.802A>T
MANE Select
|
NP_115909.1:p.Ile268Phe
|
|