ENST00000324727.9:c.564C>G
MANE Select
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ENSP00000322460.4:p.Ile188Met
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ENST00000324727.8:c.564C>G
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ENSP00000322460.4:p.Ile188Met
|
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ENST00000415030.6:n.707C>G
|
|
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ENST00000423160.2:n.198C>G
|
|
|
ENST00000529878.1:c.162C>G
|
ENSP00000436343.1:p.Ile54Met
|
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ENST00000531550.1:n.629C>G
|
|
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ENST00000532138.1:n.820C>G
|
|
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NM_001142348.1:c.162C>G
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NP_001135820.1:p.Ile54Met
|
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NM_001142349.1:c.234C>G
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NP_001135821.1:p.Ile78Met
|
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NM_174934.3:c.564C>G , LRG_330t1:c.564C>G
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NP_777594.1:p.Ile188Met
|
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NR_024527.1:n.589C>G
|
|
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NM_001142348.2:c.162C>G
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NP_001135820.1:p.Ile54Met
|
|
NM_001142349.2:c.234C>G
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NP_001135821.1:p.Ile78Met
|
|
NR_024527.2:n.553C>G
|
|
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NM_174934.4:c.564C>G
MANE Select
|
NP_777594.1:p.Ile188Met
|
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