ENST00000355832.10:c.3569T>G
MANE Select
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ENSP00000348089.5:p.Val1190Gly
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ENST00000679552.1:n.640T>G
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ENST00000679871.1:n.715T>G
|
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ENST00000679974.1:n.618T>G
|
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ENST00000681632.1:n.4972T>G
|
|
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ENST00000681659.1:c.3410T>G
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ENSP00000505631.1:p.Val1137Gly
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ENST00000355832.9:c.3569T>G
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ENSP00000348089.5:p.Val1190Gly
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ENST00000623073.3:c.*1865T>G
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ENSP00000485650.1:n.*1865T>G
|
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ENST00000623115.3:c.1679T>G
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ENSP00000485321.1:p.Val560Gly
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ENST00000624341.3:c.1401T>G
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NM_000124.3:c.3569T>G
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NP_000115.1:p.Val1190Gly
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XR_945953.1:n.243-1174A>C
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NM_001346440.1:c.3569T>G
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NP_001333369.1:p.Val1190Gly
|
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NM_000124.4:c.3569T>G
MANE Select
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NP_000115.1:p.Val1190Gly
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NM_001346440.2:c.3569T>G
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NP_001333369.1:p.Val1190Gly
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