ENST00000396705.10:c.*179G>T
MANE Select
|
ENSP00000379933.4:n.*179G>T
|
|
ENST00000229270.8:c.*179G>T
|
ENSP00000229270.4:n.*179G>T
|
|
ENST00000396705.9:c.*179G>T
|
ENSP00000379933.4:n.*179G>T
|
|
ENST00000474253.1:n.418G>T
|
|
|
ENST00000535434.5:c.*179G>T
|
ENSP00000443599.1:n.*179G>T
|
|
ENST00000613953.4:c.*179G>T
|
ENSP00000484435.1:n.*179G>T
|
|
NM_000365.5:c.*179G>T
|
NP_000356.1:n.*179G>T
|
|
NM_001159287.1:c.*179G>T
|
NP_001152759.1:n.*179G>T
|
|
NM_001258026.1:c.*179G>T
|
NP_001244955.1:n.*179G>T
|
|
XR_002957378.1:n.1937G>T
|
|
|
NM_000365.6:c.*179G>T
MANE Select
|
NP_000356.1:n.*179G>T
|
|
NM_001258026.2:c.*179G>T
|
NP_001244955.1:n.*179G>T
|
|