ENST00000355832.10:c.3957G>C
MANE Select
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ENSP00000348089.5:p.Gly1319=
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ENST00000679552.1:n.1028G>C
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ENST00000679871.1:n.1103G>C
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ENST00000679974.1:n.1006G>C
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ENST00000681632.1:n.5360G>C
|
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ENST00000681659.1:c.3798G>C
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ENSP00000505631.1:p.Gly1266=
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ENST00000355832.9:c.3957G>C
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ENSP00000348089.5:p.Gly1319=
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ENST00000465653.1:n.279G>C
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ENST00000623073.3:c.*2253G>C
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ENSP00000485650.1:n.*2253G>C
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ENST00000623115.3:c.2067G>C
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ENSP00000485321.1:p.Gly689=
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ENST00000624341.3:c.1789G>C
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NM_000124.3:c.3957G>C
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NP_000115.1:p.Gly1319=
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XR_945953.1:n.243-10187C>G
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NM_001346440.1:c.3957G>C
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NP_001333369.1:p.Gly1319=
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NM_000124.4:c.3957G>C
MANE Select
|
NP_000115.1:p.Gly1319=
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NM_001346440.2:c.3957G>C
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NP_001333369.1:p.Gly1319=
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