ENST00000393716.8:c.109G>C
MANE Select
|
ENSP00000377319.3:p.Gly37Arg
|
|
ENST00000466380.6:c.109G>C
|
ENSP00000420297.2:p.Gly37Arg
|
|
ENST00000648112.1:c.*132G>C
|
ENSP00000497876.1:n.*132G>C
|
|
ENST00000337940.4:c.226G>C
|
ENSP00000336528.4:p.Gly76Arg
|
|
ENST00000393716.6:c.109G>C
|
ENSP00000377319.2:p.Gly37Arg
|
|
ENST00000466380.5:c.109G>C
|
ENSP00000420297.1:p.Gly37Arg
|
|
ENST00000474090.1:n.397G>C
|
|
|
NM_003889.3:c.109G>C
|
NP_003880.3:p.Gly37Arg
|
|
NM_022002.2:c.226G>C
|
NP_071285.1:p.Gly76Arg
|
|
NM_033013.2:c.109G>C
|
NP_148934.1:p.Gly37Arg
|
|
NM_003889.4:c.109G>C
MANE Select
|
NP_003880.3:p.Gly37Arg
|
|
NM_022002.3:c.226G>C
|
NP_071285.1:p.Gly76Arg
|
|
NM_033013.3:c.109G>C
|
NP_148934.1:p.Gly37Arg
|
|