ENST00000391944.8:c.1396A>T
|
ENSP00000375808.4:p.Ile466Phe
|
|
ENST00000682414.1:c.1396A>T
|
ENSP00000507019.1:p.Ile466Phe
|
|
ENST00000682508.1:n.1425A>T
|
|
|
ENST00000684218.1:c.*654A>T
|
ENSP00000507804.1:n.*654A>T
|
|
ENST00000684264.1:n.952A>T
|
|
|
ENST00000684407.1:c.1273A>T
|
ENSP00000507775.1:p.Ile425Phe
|
|
ENST00000684458.1:c.1326A>T
|
ENSP00000508260.1:p.Thr442=
|
|
ENST00000684468.1:n.1172A>T
|
|
|
ENST00000391945.10:c.1396A>T
MANE Select
|
ENSP00000375809.4:p.Ile466Phe
|
|
ENST00000587376.6:c.519A>T
|
|
|
ENST00000646507.1:n.1493A>T
|
|
|
ENST00000391941.6:c.1324A>T
|
ENSP00000375805.2:p.Ile442Phe
|
|
ENST00000391942.6:n.567A>T
|
|
|
ENST00000391944.7:c.1162A>T
|
ENSP00000375808.3:p.Ile388Phe
|
|
ENST00000391945.8:c.1396A>T
|
ENSP00000375809.3:p.Ile466Phe
|
|
ENST00000587376.5:c.519A>T
|
|
|
ENST00000588652.5:n.1484A>T
|
|
|
NM_000400.3:c.1396A>T , LRG_461t1:c.1396A>T
|
NP_000391.1:p.Ile466Phe
|
|
XM_011526611.1:c.1318A>T
|
XP_011524913.1:p.Ile440Phe
|
|
XR_935763.1:n.1443A>T
|
|
|
XM_011526611.2:c.1318A>T
|
XP_011524913.1:p.Ile440Phe
|
|
XM_017026467.1:c.1273A>T
|
XP_016881956.1:p.Ile425Phe
|
|
XR_001753633.2:n.1443A>T
|
|
|
XR_001753634.2:n.1443A>T
|
|
|
NM_000400.4:c.1396A>T
MANE Select
|
NP_000391.1:p.Ile466Phe
|
|