ENST00000403733.8:c.3161T>G
MANE Select
|
ENSP00000384222.3:p.Leu1054Arg
|
|
ENST00000403733.7:c.3161T>G
|
ENSP00000384222.3:p.Leu1054Arg
|
|
ENST00000427431.5:c.*2553T>G
|
ENSP00000393342.1:n.*2553T>G
|
|
ENST00000438543.5:c.*957T>G
|
ENSP00000413521.1:n.*957T>G
|
|
ENST00000448232.6:c.3233T>G
|
ENSP00000398577.2:p.Leu1078Arg
|
|
ENST00000504005.5:c.2207T>G
|
ENSP00000427569.1:p.Leu736Arg
|
|
ENST00000508747.1:c.545T>G
|
ENSP00000420835.1:p.Leu182Arg
|
|
ENST00000513834.5:c.3014T>G
|
ENSP00000425054.1:p.Leu1005Arg
|
|
NM_024949.5:c.3161T>G
|
NP_079225.5:p.Leu1054Arg
|
|
XM_011532269.1:c.3233T>G
|
XP_011530571.1:p.Leu1078Arg
|
|
XM_011532269.3:c.3233T>G
|
XP_011530571.1:p.Leu1078Arg
|
|
XM_024454225.1:c.2939T>G
|
XP_024309993.1:p.Leu980Arg
|
|
NM_024949.6:c.3161T>G
MANE Select
|
NP_079225.5:p.Leu1054Arg
|
|