ENST00000403733.8:c.3207A>C
MANE Select
|
ENSP00000384222.3:p.Leu1069Phe
|
|
ENST00000403733.7:c.3207A>C
|
ENSP00000384222.3:p.Leu1069Phe
|
|
ENST00000427431.5:c.*2599A>C
|
ENSP00000393342.1:n.*2599A>C
|
|
ENST00000438543.5:c.*1003A>C
|
ENSP00000413521.1:n.*1003A>C
|
|
ENST00000448232.6:c.3279A>C
|
ENSP00000398577.2:p.Leu1093Phe
|
|
ENST00000504005.5:c.2253A>C
|
ENSP00000427569.1:p.Leu751Phe
|
|
ENST00000508747.1:c.591A>C
|
ENSP00000420835.1:p.Leu197Phe
|
|
ENST00000513834.5:c.3060A>C
|
ENSP00000425054.1:p.Leu1020Phe
|
|
NM_024949.5:c.3207A>C
|
NP_079225.5:p.Leu1069Phe
|
|
XM_011532269.1:c.3279A>C
|
XP_011530571.1:p.Leu1093Phe
|
|
XM_011532269.3:c.3279A>C
|
XP_011530571.1:p.Leu1093Phe
|
|
XM_024454225.1:c.2985A>C
|
XP_024309993.1:p.Leu995Phe
|
|
NM_024949.6:c.3207A>C
MANE Select
|
NP_079225.5:p.Leu1069Phe
|
|