ENST00000269373.11:c.*51_*52insCTG
MANE Select
|
ENSP00000269373.6:n.*51_*52insCTG
|
|
ENST00000269373.10:c.*51_*52insCTG
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ENSP00000269373.6:n.*51_*52insCTG
|
|
ENST00000571594.1:c.53+55_53+56insCTG
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ENSP00000459751.1:n.53+55_53+56insCTG
|
|
ENST00000574832.5:c.*938_*939insCTG
|
ENSP00000460869.1:n.*938_*939insCTG
|
|
NM_024619.3:c.*51_*52insCTG
|
NP_078895.2:n.*51_*52insCTG
|
|
NR_046408.1:n.1159_1160insCTG
|
|
|
XM_024450948.1:c.*51_*52insCTG
|
XP_024306716.1:n.*51_*52insCTG
|
|
NM_024619.4:c.*51_*52insCTG
MANE Select
|
NP_078895.2:n.*51_*52insCTG
|
|
NR_046408.2:n.1159_1160insCTG
|
|
|