ENST00000263321.6:c.770_772delinsCCA
MANE Select
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ENSP00000263321.4:p.Pro257=
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ENST00000263321.5:c.770_772delinsCCA
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ENSP00000263321.4:p.Pro257=
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|
ENST00000526139.1:n.831_833delinsCCA
|
|
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NM_000372.4:c.770_772delinsCCA
|
NP_000363.1:p.Pro257=
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|
XM_011542970.1:c.770_772delinsCCA
|
XP_011541272.1:p.Pro257=
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|
XM_011542970.2:c.770_772delinsCCA
|
XP_011541272.1:p.Pro257=
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|
XR_001748321.1:n.2718-65192_2718-65190delinsTGG
|
|
|
XR_001748322.1:n.2733-65192_2733-65190delinsTGG
|
|
|
NM_000372.5:c.770_772delinsCCA
MANE Select
|
NP_000363.1:p.Pro257=
|
|