ENST00000305046.13:c.168C>G
MANE Select
|
ENSP00000306606.8:p.Gly56=
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ENST00000639454.1:c.168C>G
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ENSP00000491622.1:p.Gly56=
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ENST00000305046.12:c.168C>G
|
ENSP00000306606.8:p.Gly56=
|
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ENST00000504498.1:n.222C>G
|
|
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ENST00000506651.5:c.48C>G
|
ENSP00000425998.2:p.Gly16=
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ENST00000515694.4:n.2263C>G
|
|
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ENST00000625860.2:c.48C>G
|
ENSP00000486614.1:p.Gly16=
|
|
ENST00000632775.1:n.731C>G
|
|
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NM_000668.5:c.168C>G
|
NP_000659.2:p.Gly56=
|
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NM_001286650.1:c.48C>G
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NP_001273579.1:p.Gly16=
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|
NM_000668.6:c.168C>G
MANE Select
|
NP_000659.2:p.Gly56=
|
|
NM_001286650.2:c.48C>G
|
NP_001273579.1:p.Gly16=
|
|