ENST00000403733.8:c.3213G>T
MANE Select
|
ENSP00000384222.3:p.Leu1071=
|
|
ENST00000403733.7:c.3213G>T
|
ENSP00000384222.3:p.Leu1071=
|
|
ENST00000427431.5:c.*2605G>T
|
ENSP00000393342.1:n.*2605G>T
|
|
ENST00000438543.5:c.*1009G>T
|
ENSP00000413521.1:n.*1009G>T
|
|
ENST00000448232.6:c.3285G>T
|
ENSP00000398577.2:p.Leu1095=
|
|
ENST00000504005.5:c.2259G>T
|
ENSP00000427569.1:p.Leu753=
|
|
ENST00000508747.1:c.597G>T
|
ENSP00000420835.1:p.Leu199=
|
|
ENST00000513834.5:c.3066G>T
|
ENSP00000425054.1:p.Leu1022=
|
|
NM_024949.5:c.3213G>T
|
NP_079225.5:p.Leu1071=
|
|
XM_011532269.1:c.3285G>T
|
XP_011530571.1:p.Leu1095=
|
|
XM_011532269.3:c.3285G>T
|
XP_011530571.1:p.Leu1095=
|
|
XM_024454225.1:c.2991G>T
|
XP_024309993.1:p.Leu997=
|
|
NM_024949.6:c.3213G>T
MANE Select
|
NP_079225.5:p.Leu1071=
|
|