ENST00000357749.7:c.703-268C=
MANE Select
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ENSP00000350386.2:n.703-268C=
|
|
ENST00000357749.6:c.703-268C=
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ENSP00000350386.2:n.703-268C=
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|
ENST00000467744.2:n.126+68246C=
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|
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NM_000390.2:c.703-268C= , LRG_699t1:c.703-268C=
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NP_000381.1:n.703-268C=
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|
XM_006724615.2:c.640-268C=
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XP_006724678.1:n.640-268C=
|
|
XM_011530839.1:c.259-268C=
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XP_011529141.1:n.259-268C=
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|
NM_000390.3:c.703-268C=
|
NP_000381.1:n.703-268C=
|
|
NM_001320959.1:c.259-268C=
|
NP_001307888.1:n.259-268C=
|
|
NM_001362517.1:c.259-268C=
|
NP_001349446.1:n.259-268C=
|
|
NM_001362518.1:c.259-268C=
|
NP_001349447.1:n.259-268C=
|
|
NM_001362519.1:c.259-268C=
|
NP_001349448.1:n.259-268C=
|
|
XM_017029242.2:c.703-268C=
|
XP_016884731.1:n.703-268C=
|
|
XM_017029246.1:c.259-268C=
|
XP_016884735.1:n.259-268C=
|
|
XM_024452331.1:c.259-268C=
|
XP_024308099.1:n.259-268C=
|
|
NM_000390.4:c.703-268C=
MANE Select
|
NP_000381.1:n.703-268C=
|
|
NM_001362518.2:c.259-268C=
|
NP_001349447.1:n.259-268C=
|
|