ENST00000262493.12:c.781A>T
MANE Select
|
ENSP00000262493.6:p.Ile261Phe
|
|
ENST00000562316.6:c.448A>T
|
ENSP00000457238.2:p.Ile150Phe
|
|
ENST00000564727.2:c.85A>T
|
ENSP00000454971.2:p.Ile29Phe
|
|
ENST00000568375.2:c.116-3425A>T
|
|
|
ENST00000638185.1:n.996A>T
|
|
|
ENST00000638210.1:n.1081A>T
|
|
|
ENST00000638705.1:c.781A>T
|
ENSP00000491223.1:p.Ile261Phe
|
|
ENST00000638836.1:n.691A>T
|
|
|
ENST00000639055.1:n.1502A>T
|
|
|
ENST00000639251.1:n.682A>T
|
|
|
ENST00000639268.1:c.416A>T
|
|
|
ENST00000639341.1:c.306A>T
|
|
|
ENST00000639770.1:c.819A>T
|
ENSP00000491999.1:n.819A>T
|
|
ENST00000640390.1:n.711A>T
|
|
|
ENST00000640469.1:c.145A>T
|
ENSP00000491875.1:p.Ile49Phe
|
|
ENST00000640560.1:n.557A>T
|
|
|
ENST00000640893.1:c.*179A>T
|
ENSP00000492677.1:n.*179A>T
|
|
ENST00000262493.10:c.781A>T
|
ENSP00000262493.6:p.Ile261Phe
|
|
ENST00000564727.1:c.1A>T
|
ENSP00000454971.1:p.Ile1Phe
|
|
ENST00000568375.1:n.116-3425A>T
|
|
|
NM_020988.2:c.781A>T
|
NP_066268.1:p.Ile261Phe
|
|
XM_011523003.1:c.655A>T
|
XP_011521305.1:p.Ile219Phe
|
|
XM_011523003.3:c.655A>T
|
XP_011521305.1:p.Ile219Phe
|
|
NM_020988.3:c.781A>T
MANE Select
|
NP_066268.1:p.Ile261Phe
|
|