ENST00000455537.7:c.2934T>G
MANE Select
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ENSP00000408979.2:p.Ser978Arg
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ENST00000674619.1:c.2955T>G
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ENSP00000502270.1:p.Ser985Arg
|
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ENST00000675697.1:c.25T>G
|
|
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ENST00000675737.1:n.338T>G
|
|
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ENST00000675882.1:n.2457T>G
|
|
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ENST00000675929.1:n.1492T>G
|
|
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ENST00000676055.1:c.25T>G
|
|
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ENST00000676457.1:c.2829T>G
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ENSP00000501588.1:p.Ser943Arg
|
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ENST00000286452.5:c.2667T>G
|
ENSP00000286452.5:p.Ser889Arg
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ENST00000455537.6:c.2934T>G
|
ENSP00000408979.2:p.Ser978Arg
|
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ENST00000552227.1:n.217T>G
|
|
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NM_004984.2:c.2934T>G
|
NP_004975.2:p.Ser978Arg
|
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NM_001354705.1:c.2667T>G
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NP_001341634.1:p.Ser889Arg
|
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NM_004984.3:c.2934T>G
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NP_004975.2:p.Ser978Arg
|
|
XR_002957324.1:n.3167T>G
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|
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NM_004984.4:c.2934T>G
MANE Select
|
NP_004975.2:p.Ser978Arg
|
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NM_001354705.2:c.2667T>G
|
NP_001341634.1:p.Ser889Arg
|
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