ENST00000403733.8:c.3206T>A
MANE Select
|
ENSP00000384222.3:p.Leu1069Ter
|
|
ENST00000403733.7:c.3206T>A
|
ENSP00000384222.3:p.Leu1069Ter
|
|
ENST00000427431.5:c.*2598T>A
|
ENSP00000393342.1:n.*2598T>A
|
|
ENST00000438543.5:c.*1002T>A
|
ENSP00000413521.1:n.*1002T>A
|
|
ENST00000448232.6:c.3278T>A
|
ENSP00000398577.2:p.Leu1093Ter
|
|
ENST00000504005.5:c.2252T>A
|
ENSP00000427569.1:p.Leu751Ter
|
|
ENST00000508747.1:c.590T>A
|
ENSP00000420835.1:p.Leu197Ter
|
|
ENST00000513834.5:c.3059T>A
|
ENSP00000425054.1:p.Leu1020Ter
|
|
NM_024949.5:c.3206T>A
|
NP_079225.5:p.Leu1069Ter
|
|
XM_011532269.1:c.3278T>A
|
XP_011530571.1:p.Leu1093Ter
|
|
XM_011532269.3:c.3278T>A
|
XP_011530571.1:p.Leu1093Ter
|
|
XM_024454225.1:c.2984T>A
|
XP_024309993.1:p.Leu995Ter
|
|
NM_024949.6:c.3206T>A
MANE Select
|
NP_079225.5:p.Leu1069Ter
|
|