ENST00000331373.10:c.918G>T
MANE Select
|
ENSP00000331258.5:p.Leu306Phe
|
|
ENST00000614426.2:c.*714G>T
|
ENSP00000478821.2:n.*714G>T
|
|
ENST00000674646.1:c.636G>T
|
ENSP00000501703.1:p.Leu212Phe
|
|
ENST00000674676.1:c.636G>T
|
ENSP00000502544.1:p.Leu212Phe
|
|
ENST00000674782.1:c.*838G>T
|
ENSP00000501683.1:n.*838G>T
|
|
ENST00000674937.1:c.876G>T
|
ENSP00000501823.1:p.Leu292Phe
|
|
ENST00000675322.1:c.636G>T
|
ENSP00000502235.1:p.Leu212Phe
|
|
ENST00000675675.1:c.636G>T
|
ENSP00000501793.1:p.Leu212Phe
|
|
ENST00000676178.1:c.*703G>T
|
ENSP00000502007.1:n.*703G>T
|
|
ENST00000676193.1:c.918G>T
|
ENSP00000502774.1:p.Leu306Phe
|
|
ENST00000331373.9:c.918G>T
|
ENSP00000331258.5:p.Leu306Phe
|
|
ENST00000614426.1:c.918G>T
|
ENSP00000478821.1:p.Leu306Phe
|
|
NM_001277971.1:c.918G>T
|
NP_001264900.1:p.Leu306Phe
|
|
NM_032237.4:c.918G>T
|
NP_115613.1:p.Leu306Phe
|
|
XM_011544668.1:c.918G>T
|
XP_011542970.1:p.Leu306Phe
|
|
XM_011544669.1:c.918G>T
|
XP_011542971.1:p.Leu306Phe
|
|
NM_032237.5:c.918G>T
MANE Select
|
NP_115613.1:p.Leu306Phe
|
|
NM_001277971.2:c.918G>T
|
NP_001264900.1:p.Leu306Phe
|
|