ENST00000393716.8:c.-2A>C
MANE Select
|
ENSP00000377319.3:n.-2A>C
|
|
ENST00000466380.6:c.-2A>C
|
ENSP00000420297.2:n.-2A>C
|
|
ENST00000648112.1:c.*22A>C
|
ENSP00000497876.1:n.*22A>C
|
|
ENST00000337940.4:c.116A>C
|
ENSP00000336528.4:p.Asn39Thr
|
|
ENST00000393716.6:c.-2A>C
|
ENSP00000377319.2:n.-2A>C
|
|
ENST00000466380.5:c.-2A>C
|
ENSP00000420297.1:n.-2A>C
|
|
ENST00000474090.1:n.287A>C
|
|
|
NM_003889.3:c.-2A>C
|
NP_003880.3:n.-2A>C
|
|
NM_022002.2:c.116A>C
|
NP_071285.1:p.Asn39Thr
|
|
NM_033013.2:c.-2A>C
|
NP_148934.1:n.-2A>C
|
|
NM_003889.4:c.-2A>C
MANE Select
|
NP_003880.3:n.-2A>C
|
|
NM_022002.3:c.116A>C
|
NP_071285.1:p.Asn39Thr
|
|
NM_033013.3:c.-2A>C
|
NP_148934.1:n.-2A>C
|
|