ENST00000621467.5:c.*999A>G
(TMEM237)
|
ENSP00000480508.2:n.*999A>G
|
|
ENST00000686475.1:n.2166A>G
(TMEM237)
|
|
|
ENST00000409883.7:c.*999A>G
(TMEM237)
MANE Select
|
ENSP00000386264.2:n.*999A>G
|
|
ENST00000409444.6:c.*999A>G
(TMEM237)
|
ENSP00000387203.2:n.*999A>G
|
|
ENST00000409883.6:c.*999A>G
(TMEM237)
|
ENSP00000386264.2:n.*999A>G
|
|
ENST00000416471.2:n.175A>G
(ENO1P4)
|
|
|
ENST00000495329.1:n.1365A>G
(TMEM237)
|
|
|
NM_001044385.2:c.*999A>G
(TMEM237)
|
NP_001037850.1:n.*999A>G
|
|
NM_152388.3:c.*999A>G
(TMEM237)
|
NP_689601.2:n.*999A>G
|
|
NM_001044385.3:c.*999A>G
(TMEM237)
MANE Select
|
NP_001037850.1:n.*999A>G
|
|
NM_152388.4:c.*999A>G
(TMEM237)
|
NP_689601.2:n.*999A>G
|
|