ENST00000328300.11:c.4195del
MANE Select
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ENSP00000331902.7:p.Gln1399LysfsTer?
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ENST00000361603.7:c.4177del
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ENSP00000354505.2:p.Gln1393LysfsTer?
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ENST00000510690.2:n.689del
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|
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ENST00000328300.10:c.4195del
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ENSP00000331902.6:p.Gln1399LysfsTer?
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ENST00000361603.6:c.4177del
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ENSP00000354505.2:p.Gln1393LysfsTer?
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ENST00000489230.1:n.598del
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|
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NM_000495.4:c.4177del
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NP_000486.1:p.Gln1393LysfsTer?
|
|
NM_033380.2:c.4195del
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NP_203699.1:p.Gln1399LysfsTer?
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XM_005262070.2:c.4186del
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XP_005262127.1:p.Gln1396LysfsTer?
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|
XM_006724616.2:c.4195del
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XP_006724679.1:p.Gln1399LysfsTer?
|
|
XM_011530849.1:c.3871del
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XP_011529151.1:p.Gln1291LysfsTer?
|
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XM_011530851.1:c.1768del
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XP_011529153.1:p.Gln590LysfsTer?
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|
XM_011530849.2:c.4210del
|
XP_011529151.2:p.Gln1404LysfsTer?
|
|
XM_017029259.2:c.4201del
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XP_016884748.1:p.Gln1401LysfsTer?
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|
XM_017029260.1:c.4192del
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XP_016884749.1:p.Gln1398LysfsTer?
|
|
XM_017029263.2:c.2530del
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XP_016884752.1:p.Gln844LysfsTer?
|
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NM_000495.5:c.4177del
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NP_000486.1:p.Gln1393LysfsTer?
|
|
NM_033380.3:c.4195del
MANE Select
|
NP_203699.1:p.Gln1399LysfsTer?
|
|