ENST00000617979.5:c.237+186G>C
MANE Select
|
ENSP00000483375.1:n.237+186G>C
|
|
ENST00000374497.7:c.237+186G>C
|
ENSP00000363621.3:n.237+186G>C
|
|
ENST00000418277.5:c.45+186G>C
|
ENSP00000414719.1:n.45+186G>C
|
|
ENST00000425913.5:c.237+186G>C
|
ENSP00000393359.1:n.237+186G>C
|
|
ENST00000429356.5:c.45+186G>C
|
ENSP00000398585.1:n.45+186G>C
|
|
ENST00000445705.1:c.237+186G>C
|
ENSP00000398257.1:n.237+186G>C
|
|
ENST00000459934.5:n.355+186G>C
|
|
|
ENST00000466250.5:n.549G>C
|
|
|
ENST00000467493.5:n.499G>C
|
|
|
ENST00000470383.1:n.1971G>C
|
|
|
ENST00000470949.5:n.187+186G>C
|
|
|
ENST00000481736.5:n.443G>C
|
|
|
ENST00000486382.1:n.343+186G>C
|
|
|
ENST00000617979.4:c.237+186G>C
|
ENSP00000483375.1:n.237+186G>C
|
|
NM_000403.3:c.237+186G>C
|
NP_000394.2:n.237+186G>C
|
|
NM_001008216.1:c.237+186G>C
|
NP_001008217.1:n.237+186G>C
|
|
NM_001127621.1:c.237+186G>C
|
NP_001121093.1:n.237+186G>C
|
|
NM_001008216.2:c.237+186G>C
MANE Select
|
NP_001008217.1:n.237+186G>C
|
|
NM_000403.4:c.237+186G>C
|
NP_000394.2:n.237+186G>C
|
|
NM_001127621.2:c.237+186G>C
|
NP_001121093.1:n.237+186G>C
|
|