ENST00000243964.7:c.3017T>G
MANE Select
|
ENSP00000243964.4:p.Leu1006Arg
|
|
ENST00000243964.6:c.3017T>G
|
ENSP00000243964.3:p.Leu1006Arg
|
|
ENST00000454036.6:c.3086T>G
|
ENSP00000387694.1:p.Leu1029Arg
|
|
ENST00000616201.4:c.1298-2185T>G
|
ENSP00000484585.1:n.1298-2185T>G
|
|
ENST00000616202.4:c.613-2010T>G
|
ENSP00000478369.1:n.613-2010T>G
|
|
ENST00000616933.4:c.*2335T>G
|
ENSP00000477569.1:n.*2335T>G
|
|
ENST00000626937.2:c.510-3128T>G
|
ENSP00000485953.1:n.510-3128T>G
|
|
ENST00000628413.1:n.533T>G
|
|
|
NM_001134771.1:c.3086T>G
|
NP_001128243.1:p.Leu1029Arg
|
|
NM_020708.4:c.3017T>G
|
NP_065759.1:p.Leu1006Arg
|
|
XM_017027981.1:c.3086T>G
|
XP_016883470.1:p.Leu1029Arg
|
|
NM_001134771.2:c.3086T>G
|
NP_001128243.1:p.Leu1029Arg
|
|
NM_020708.5:c.3017T>G
MANE Select
|
NP_065759.1:p.Leu1006Arg
|
|