ENST00000578493.2:n.707_711delinsTTACC
|
|
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ENST00000699291.1:c.499_503delinsTTACC
|
ENSP00000514272.1:p.Leu167=
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ENST00000699292.1:n.414_418delinsTTACC
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|
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ENST00000225275.4:c.1374_1378delinsTTACC
MANE Select
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ENSP00000225275.3:p.Thr458=
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ENST00000225275.3:c.1374_1378delinsTTACC
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ENSP00000225275.3:p.Thr458=
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|
NM_000250.1:c.1374_1378delinsTTACC , LRG_84t1:c.1374_1378delinsTTACC
|
NP_000241.1:p.Thr458=
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|
XM_011524821.1:c.1560_1564delinsTTACC
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XP_011523123.1:p.Thr520=
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|
XM_011524822.1:c.1089_1093delinsTTACC
|
XP_011523124.1:p.Thr363=
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|
XM_011524823.1:c.1399_1403delinsTTACC
|
XP_011523125.1:p.Leu467=
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NM_000250.2:c.1374_1378delinsTTACC
MANE Select
|
NP_000241.1:p.Thr458=
|
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