ENST00000594866.3:c.1247C>G
MANE Select
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ENSP00000469738.2:p.Ala416Gly
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ENST00000614245.2:c.521C>G
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ENSP00000480219.2:p.Ala174Gly
|
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ENST00000396720.7:c.1247C>G
|
ENSP00000379946.2:p.Ala416Gly
|
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ENST00000614245.1:c.1091C>G
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ENSP00000480219.1:p.Ala364Gly
|
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NM_015711.3:c.1247C>G
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NP_056526.3:p.Ala416Gly
|
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XM_005258833.3:c.1247C>G
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XP_005258890.1:p.Ala416Gly
|
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XM_006723180.2:c.1247C>G
|
XP_006723243.1:p.Ala416Gly
|
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XM_011526882.1:c.1109C>G
|
XP_011525184.1:p.Ala370Gly
|
|
XM_011526883.1:c.1247C>G
|
XP_011525185.1:p.Ala416Gly
|
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XM_005258833.4:c.1247C>G
|
XP_005258890.1:p.Ala416Gly
|
|
XM_006723180.3:c.1247C>G
|
XP_006723243.1:p.Ala416Gly
|
|
XM_011526882.2:c.1109C>G
|
XP_011525184.1:p.Ala370Gly
|
|
XM_011526883.2:c.1247C>G
|
XP_011525185.1:p.Ala416Gly
|
|
NM_001394372.1:c.1247C>G
MANE Select
|
NP_001381301.1:p.Ala416Gly
|
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