ENST00000265512.12:c.*13del
MANE Select
|
ENSP00000265512.7:n.*13del
|
|
ENST00000265512.11:c.*13del
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ENSP00000265512.7:n.*13del
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|
ENST00000505590.5:c.*13del
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ENSP00000425416.1:n.*13del
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|
ENST00000508393.5:c.*13del
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ENSP00000424630.1:n.*13del
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|
ENST00000509471.5:c.510del
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ENSP00000424583.1:n.510del
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|
ENST00000629236.2:c.1153del
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ENSP00000486450.1:p.Gln385AsnfsTer20
|
|
NM_000670.3:c.*13del
|
NP_000661.2:n.*13del
|
|
NM_000670.4:c.*13del
|
NP_000661.2:n.*13del
|
|
NM_001306171.1:c.*13del
|
NP_001293100.1:n.*13del
|
|
NM_001306172.1:c.*13del
|
NP_001293101.1:n.*13del
|
|
NR_037884.1:n.429-9126del
|
|
|
XR_938685.1:n.1495del
|
|
|
XR_938686.1:n.1486del
|
|
|
XR_938687.1:n.1359del
|
|
|
NM_000670.5:c.*13del
MANE Select
|
NP_000661.2:n.*13del
|
|
NM_001306171.2:c.*13del
|
NP_001293100.1:n.*13del
|
|
NM_001306172.2:c.*13del
|
NP_001293101.1:n.*13del
|
|