ENST00000593677.2:c.1850del
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|
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ENST00000688602.1:c.3247del
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|
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ENST00000689936.1:c.3219del
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|
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ENST00000692547.1:n.307del
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ENST00000359596.8:c.14914del
MANE Select
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ENSP00000352608.2:p.Thr4972HisfsTer22
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ENST00000355481.8:c.14899del
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ENSP00000347667.3:p.Thr4967HisfsTer22
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ENST00000359596.7:c.14914del
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ENSP00000352608.2:p.Thr4972HisfsTer22
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ENST00000360985.7:c.14896del
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ENSP00000354254.4:p.Thr4966HisfsTer22
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NM_000540.2:c.14914del , LRG_766t1:c.14914del
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NP_000531.2:p.Thr4972HisfsTer22
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NM_001042723.1:c.14899del
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NP_001036188.1:p.Thr4967HisfsTer22
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|
XM_006723317.1:c.14896del
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XP_006723380.1:p.Thr4966HisfsTer22
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|
XM_006723319.1:c.14881del
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XP_006723382.1:p.Thr4961HisfsTer22
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|
XM_011527204.1:c.14911del
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XP_011525506.1:p.Thr4971HisfsTer22
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|
XM_011527205.1:c.14827del
|
XP_011525507.1:p.Thr4943HisfsTer22
|
|
XM_006723317.2:c.14896del
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XP_006723380.1:p.Thr4966HisfsTer22
|
|
XM_006723319.2:c.14881del
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XP_006723382.1:p.Thr4961HisfsTer22
|
|
XM_011527205.2:c.14827del
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XP_011525507.1:p.Thr4943HisfsTer22
|
|
NM_000540.3:c.14914del
MANE Select
|
NP_000531.2:p.Thr4972HisfsTer22
|
|
NM_001042723.2:c.14899del
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NP_001036188.1:p.Thr4967HisfsTer22
|
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