ENST00000300060.7:c.2247C=
MANE Select
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ENSP00000300060.6:p.Asp749=
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ENST00000559874.2:c.2247C=
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ENSP00000452934.2:p.Asp749=
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ENST00000560137.2:c.2247C=
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ENSP00000453413.2:p.Asp749=
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ENST00000679248.1:c.2247C=
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ENSP00000502886.1:p.Asp749=
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ENST00000300060.6:c.2247C=
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ENSP00000300060.6:p.Asp749=
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ENST00000558740.1:n.151C=
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|
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NM_001150.2:c.2247C=
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NP_001141.2:p.Asp749=
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XM_005254892.3:c.2247C=
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XP_005254949.1:p.Asp749=
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XM_011521473.1:c.2247C=
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XP_011519775.1:p.Asp749=
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XM_011521474.1:c.*80C=
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XP_011519776.1:n.*80C=
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|
XM_005254892.4:c.2247C=
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XP_005254949.1:p.Asp749=
|
|
NM_001150.3:c.2247C=
MANE Select
|
NP_001141.2:p.Asp749=
|
|
NM_001381923.1:c.2247C=
|
NP_001368852.1:p.Asp749=
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NM_001381924.1:c.2247C=
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NP_001368853.1:p.Asp749=
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|