ENST00000393716.8:c.-4A>G
MANE Select
|
ENSP00000377319.3:n.-4A>G
|
|
ENST00000466380.6:c.-4A>G
|
ENSP00000420297.2:n.-4A>G
|
|
ENST00000648112.1:c.*20A>G
|
ENSP00000497876.1:n.*20A>G
|
|
ENST00000337940.4:c.114A>G
|
ENSP00000336528.4:p.Ala38=
|
|
ENST00000393716.6:c.-4A>G
|
ENSP00000377319.2:n.-4A>G
|
|
ENST00000466380.5:c.-4A>G
|
ENSP00000420297.1:n.-4A>G
|
|
ENST00000474090.1:n.285A>G
|
|
|
NM_003889.3:c.-4A>G
|
NP_003880.3:n.-4A>G
|
|
NM_022002.2:c.114A>G
|
NP_071285.1:p.Ala38=
|
|
NM_033013.2:c.-4A>G
|
NP_148934.1:n.-4A>G
|
|
NM_003889.4:c.-4A>G
MANE Select
|
NP_003880.3:n.-4A>G
|
|
NM_022002.3:c.114A>G
|
NP_071285.1:p.Ala38=
|
|
NM_033013.3:c.-4A>G
|
NP_148934.1:n.-4A>G
|
|