ENST00000375190.10:c.837C>G
MANE Select
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ENSP00000364336.4:p.Ala279=
|
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ENST00000375190.8:c.837C>G
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ENSP00000364336.3:p.Ala279=
|
|
ENST00000411851.3:c.837C>G
|
ENSP00000393333.2:p.Ala279=
|
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ENST00000589966.1:c.448C>G
|
ENSP00000468145.1:p.Arg150Gly
|
|
NM_001060.5:c.837C>G , LRG_578t1:c.837C>G
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NP_001051.1:p.Ala279=
|
|
NM_201636.2:c.837C>G
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NP_963998.2:p.Ala279=
|
|
XM_011528214.1:c.837C>G
|
XP_011526516.1:p.Ala279=
|
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XM_011528214.2:c.837C>G
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XP_011526516.1:p.Ala279=
|
|
NM_001060.6:c.837C>G
MANE Select
|
NP_001051.1:p.Ala279=
|
|
NM_201636.3:c.837C>G
|
NP_963998.2:p.Ala279=
|
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