ENST00000617979.5:c.238-141G>A
MANE Select
|
ENSP00000483375.1:n.238-141G>A
|
|
ENST00000374497.7:c.238-141G>A
|
ENSP00000363621.3:n.238-141G>A
|
|
ENST00000418277.5:c.46-141G>A
|
ENSP00000414719.1:n.46-141G>A
|
|
ENST00000425913.5:c.238-141G>A
|
ENSP00000393359.1:n.238-141G>A
|
|
ENST00000429356.5:c.46-141G>A
|
ENSP00000398585.1:n.46-141G>A
|
|
ENST00000445705.1:c.238-141G>A
|
ENSP00000398257.1:n.238-141G>A
|
|
ENST00000459934.5:n.356-141G>A
|
|
|
ENST00000467493.5:n.557G>A
|
|
|
ENST00000470383.1:n.2029G>A
|
|
|
ENST00000470949.5:n.188-146G>A
|
|
|
ENST00000481736.5:n.501G>A
|
|
|
ENST00000486382.1:n.344-146G>A
|
|
|
ENST00000617979.4:c.238-141G>A
|
ENSP00000483375.1:n.238-141G>A
|
|
NM_000403.3:c.238-141G>A
|
NP_000394.2:n.238-141G>A
|
|
NM_001008216.1:c.238-141G>A
|
NP_001008217.1:n.238-141G>A
|
|
NM_001127621.1:c.238-141G>A
|
NP_001121093.1:n.238-141G>A
|
|
NM_001008216.2:c.238-141G>A
MANE Select
|
NP_001008217.1:n.238-141G>A
|
|
NM_000403.4:c.238-141G>A
|
NP_000394.2:n.238-141G>A
|
|
NM_001127621.2:c.238-141G>A
|
NP_001121093.1:n.238-141G>A
|
|