ENST00000305046.13:c.135A>T
MANE Select
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ENSP00000306606.8:p.Gly45=
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ENST00000639454.1:c.135A>T
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ENSP00000491622.1:p.Gly45=
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ENST00000305046.12:c.135A>T
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ENSP00000306606.8:p.Gly45=
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ENST00000504498.1:n.189A>T
|
|
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ENST00000506651.5:c.15A>T
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ENSP00000425998.2:p.Gly5=
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ENST00000515694.4:n.2230A>T
|
|
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ENST00000625860.2:c.15A>T
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ENSP00000486614.1:p.Gly5=
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ENST00000632775.1:n.698A>T
|
|
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NM_000668.5:c.135A>T
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NP_000659.2:p.Gly45=
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NM_001286650.1:c.15A>T
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NP_001273579.1:p.Gly5=
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NM_000668.6:c.135A>T
MANE Select
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NP_000659.2:p.Gly45=
|
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NM_001286650.2:c.15A>T
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NP_001273579.1:p.Gly5=
|
|