ENST00000369085.8:c.567_577delinsTTCCTCCGGCA
MANE Select
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ENSP00000358081.4:p.Pro189=
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ENST00000369085.7:c.567_577delinsTTCCTCCGGCA
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ENSP00000358081.3:p.Pro189=
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ENST00000450186.1:c.393_403delinsTTCCTCCGGCA
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ENSP00000410036.1:p.Pro131=
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NM_004281.3:c.567_577delinsTTCCTCCGGCA , LRG_742t1:c.567_577delinsTTCCTCCGGCA
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NP_004272.2:p.Pro189=
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XM_005270287.1:c.567_577delinsTTCCTCCGGCA
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XP_005270344.1:p.Pro189=
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XM_005270287.2:c.567_577delinsTTCCTCCGGCA
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XP_005270344.1:p.Pro189=
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NM_004281.4:c.567_577delinsTTCCTCCGGCA
MANE Select
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NP_004272.2:p.Pro189=
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