ENST00000502613.3:c.1231+118C>G
MANE Select
|
ENSP00000424668.2:n.1231+118C>G
|
|
ENST00000335016.9:c.1231+118C>G
|
ENSP00000334836.5:n.1231+118C>G
|
|
ENST00000389010.7:c.*207+118C>G
|
ENSP00000373662.3:n.*207+118C>G
|
|
ENST00000502613.1:c.308+118C>G
|
|
|
ENST00000502871.5:c.1231+118C>G
|
ENSP00000421768.1:n.1231+118C>G
|
|
ENST00000628286.1:c.*207+118C>G
|
ENSP00000487317.1:n.*207+118C>G
|
|
NM_017593.3:c.1231+118C>G
|
NP_060063.2:n.1231+118C>G
|
|
NM_198892.1:c.1231+118C>G
|
NP_942595.1:n.1231+118C>G
|
|
XM_005263117.1:c.1231+118C>G
|
XP_005263174.1:n.1231+118C>G
|
|
XM_011532101.1:c.991+118C>G
|
XP_011530403.1:n.991+118C>G
|
|
XM_011532102.1:c.1231+118C>G
|
XP_011530404.1:n.1231+118C>G
|
|
XM_017008381.1:c.991+118C>G
|
XP_016863870.1:n.991+118C>G
|
|
XM_017008382.1:c.343+118C>G
|
XP_016863871.1:n.343+118C>G
|
|
NM_017593.4:c.1231+118C>G
|
NP_060063.2:n.1231+118C>G
|
|
NM_017593.5:c.1231+118C>G
|
NP_060063.2:n.1231+118C>G
|
|
NM_198892.2:c.1231+118C>G
MANE Select
|
NP_942595.1:n.1231+118C>G
|
|