ENST00000355832.10:c.2976A>G
MANE Select
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ENSP00000348089.5:p.Gln992=
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ENST00000679552.1:n.142-180A>G
|
|
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ENST00000679871.1:n.122A>G
|
|
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ENST00000679974.1:n.120-180A>G
|
|
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ENST00000681632.1:n.4379A>G
|
|
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ENST00000681659.1:c.2817A>G
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ENSP00000505631.1:p.Gln939=
|
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ENST00000355832.9:c.2976A>G
|
ENSP00000348089.5:p.Gln992=
|
|
ENST00000623073.3:c.*1272A>G
|
ENSP00000485650.1:n.*1272A>G
|
|
ENST00000623115.3:c.1086A>G
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ENSP00000485321.1:p.Gln362=
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ENST00000624341.3:c.808A>G
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NM_000124.3:c.2976A>G
|
NP_000115.1:p.Gln992=
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XR_945953.1:n.243-496T>C
|
|
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NM_001346440.1:c.2976A>G
|
NP_001333369.1:p.Gln992=
|
|
NM_000124.4:c.2976A>G
MANE Select
|
NP_000115.1:p.Gln992=
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NM_001346440.2:c.2976A>G
|
NP_001333369.1:p.Gln992=
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