ENST00000261381.7:c.1735_1737delinsTTC
MANE Select
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ENSP00000261381.6:p.Phe579=
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ENST00000261381.6:c.1735_1737delinsTTC
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ENSP00000261381.6:p.Phe579=
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NM_022166.3:c.1735_1737delinsTTC
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NP_071449.1:p.Phe579=
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XM_011522574.1:c.1735_1737delinsTTC
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XP_011520876.1:p.Phe579=
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XR_933141.1:n.315_317delinsGAA
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NR_135179.1:n.287_289delinsGAA
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XM_017023539.2:c.1735_1737delinsTTC
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XP_016879028.1:p.Phe579=
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XM_017023540.2:c.1735_1737delinsTTC
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XP_016879029.1:p.Phe579=
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NM_022166.4:c.1735_1737delinsTTC
MANE Select
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NP_071449.1:p.Phe579=
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