ENST00000403733.8:c.3270G=
MANE Select
|
ENSP00000384222.3:p.Leu1090=
|
|
ENST00000403733.7:c.3270G=
|
ENSP00000384222.3:p.Leu1090=
|
|
ENST00000427431.5:c.*2662G=
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ENSP00000393342.1:n.*2662G=
|
|
ENST00000438543.5:c.*1066G=
|
ENSP00000413521.1:n.*1066G=
|
|
ENST00000448232.6:c.3342G=
|
ENSP00000398577.2:p.Leu1114=
|
|
ENST00000504005.5:c.2316G=
|
ENSP00000427569.1:p.Leu772=
|
|
ENST00000508747.1:c.654G=
|
ENSP00000420835.1:p.Leu218=
|
|
ENST00000513834.5:c.3123G=
|
ENSP00000425054.1:p.Leu1041=
|
|
NM_024949.5:c.3270G=
|
NP_079225.5:p.Leu1090=
|
|
XM_011532269.1:c.3342G=
|
XP_011530571.1:p.Leu1114=
|
|
XM_011532269.3:c.3342G=
|
XP_011530571.1:p.Leu1114=
|
|
XM_024454225.1:c.3048G=
|
XP_024309993.1:p.Leu1016=
|
|
NM_024949.6:c.3270G=
MANE Select
|
NP_079225.5:p.Leu1090=
|
|