ENST00000272286.4:c.1792T>G
MANE Select
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ENSP00000272286.2:p.Trp598Gly
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ENST00000272286.2:c.1792T>G
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ENSP00000272286.2:p.Trp598Gly
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NM_022437.2:c.1792T>G
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NP_071882.1:p.Trp598Gly
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XM_005264483.2:c.1789T>G
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XP_005264540.1:p.Trp597Gly
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XM_011533029.1:c.1804T>G
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XP_011531331.1:p.Trp602Gly
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XM_011533030.1:c.1801T>G
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XP_011531332.1:p.Trp601Gly
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XM_011533031.1:c.1576T>G
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XP_011531333.1:p.Trp526Gly
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XR_939707.1:n.2294T>G
|
|
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NM_001357321.1:c.1789T>G
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NP_001344250.1:p.Trp597Gly
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XM_011533029.2:c.1804T>G
|
XP_011531331.1:p.Trp602Gly
|
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XM_011533030.2:c.1801T>G
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XP_011531332.1:p.Trp601Gly
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XR_001738891.1:n.2308T>G
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|
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XR_939707.2:n.2308T>G
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|
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NM_022437.3:c.1792T>G
MANE Select
|
NP_071882.1:p.Trp598Gly
|
|
NM_001357321.2:c.1789T>G
|
NP_001344250.1:p.Trp597Gly
|
|