ENST00000269980.7:c.437C>G
MANE Select
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ENSP00000269980.2:p.Ala146Gly
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ENST00000269980.6:c.437C>G
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ENSP00000269980.2:p.Ala146Gly
|
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ENST00000457836.6:c.371C>G
|
ENSP00000416000.2:p.Ala124Gly
|
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ENST00000538423.5:n.563C>G
|
|
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ENST00000540732.3:c.539C>G
|
ENSP00000443246.1:p.Ala180Gly
|
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ENST00000541315.1:c.244C>G
|
|
|
ENST00000542943.5:c.350C>G
|
ENSP00000440345.1:p.Ala117Gly
|
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ENST00000595085.5:c.437C>G
|
ENSP00000471150.2:p.Ala146Gly
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NM_000709.3:c.437C>G
|
NP_000700.1:p.Ala146Gly
|
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NM_001164783.1:c.437C>G
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NP_001158255.1:p.Ala146Gly
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NM_000709.4:c.437C>G
MANE Select
|
NP_000700.1:p.Ala146Gly
|
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NM_001164783.2:c.437C>G
|
NP_001158255.1:p.Ala146Gly
|
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