ENST00000396926.8:c.*219G>T
MANE Select
|
ENSP00000380132.3:n.*219G>T
|
|
ENST00000174653.3:c.*219G>T
|
ENSP00000174653.3:n.*219G>T
|
|
ENST00000396926.7:c.*219G>T
|
ENSP00000380132.3:n.*219G>T
|
|
ENST00000518421.5:c.*219G>T
|
ENSP00000428787.1:n.*219G>T
|
|
ENST00000520689.1:c.366G>T
|
ENSP00000429804.1:n.366G>T
|
|
NM_001134296.1:c.*219G>T
|
NP_001127768.1:n.*219G>T
|
|
NM_006803.3:c.*219G>T
|
NP_006794.1:n.*219G>T
|
|
XM_017012977.2:c.*219G>T
|
XP_016868466.1:n.*219G>T
|
|
XR_001745459.2:n.1761G>T
|
|
|
NM_006803.4:c.*219G>T
MANE Select
|
NP_006794.1:n.*219G>T
|
|
NM_001134296.2:c.*219G>T
|
NP_001127768.1:n.*219G>T
|
|