ENST00000331782.8:c.1576del
MANE Select
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ENSP00000328169.3:p.Gln526ArgfsTer?
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ENST00000331782.7:c.1576del
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ENSP00000328169.3:p.Gln526ArgfsTer?
|
|
ENST00000347004.2:c.1462del
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ENSP00000328566.2:p.Gln488ArgfsTer?
|
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NM_002226.4:c.1576del
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NP_002217.3:p.Gln526ArgfsTer?
|
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NM_145159.2:c.1462del
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NP_660142.1:p.Gln488ArgfsTer?
|
|
XM_011536736.1:c.1576del
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XP_011535038.1:p.Gln526ArgfsTer?
|
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XR_001750303.2:n.1637del
|
|
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NM_002226.5:c.1576del
MANE Select
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NP_002217.3:p.Gln526ArgfsTer?
|
|
NM_145159.3:c.1462del
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NP_660142.1:p.Gln488ArgfsTer?
|
|