ENST00000312184.6:c.19G>C
MANE Select
|
ENSP00000312599.5:p.Gly7Arg
|
|
ENST00000312184.5:c.19G>C
|
ENSP00000312599.5:p.Gly7Arg
|
|
ENST00000416961.6:c.19G>C
|
ENSP00000407695.2:p.Gly7Arg
|
|
ENST00000517439.1:c.19G>C
|
ENSP00000429467.1:p.Gly7Arg
|
|
ENST00000517614.1:n.82G>C
|
|
|
ENST00000520167.5:n.317+339G>C
|
|
|
ENST00000523794.1:n.575-5G>C
|
|
|
NM_001040613.2:c.19G>C
|
NP_001035703.1:p.Gly7Arg
|
|
NM_017866.5:c.19G>C
|
NP_060336.3:p.Gly7Arg
|
|
NR_033334.1:n.159G>C
|
|
|
NM_017866.6:c.19G>C
MANE Select
|
NP_060336.3:p.Gly7Arg
|
|
NM_001040613.3:c.19G>C
|
NP_001035703.1:p.Gly7Arg
|
|
NR_033334.2:n.106G>C
|
|
|