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ENST00000544898.6:c.693T=
MANE Select
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|
|
NM_001172645.1:c.639T=
|
NP_001166116.1:p.Pro213=
|
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NM_001271934.1:c.546T=
|
NP_001258863.1:p.Pro182=
|
|
NM_001271935.1:c.431T=
|
NP_001258864.1:p.Leu144=
|
|
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|
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|
|
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|
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|
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|
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|
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|
|
NM_001272050.2:c.402T=
|
NP_001258979.1:p.Pro134=
|
|
NM_004614.5:c.693T=
MANE Select
|
NP_004605.4:p.Pro231=
|
|
NR_073520.2:n.1682T=
|
|
|
NM_001172645.2:c.639T=
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|
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