ENST00000559133.6:c.6592C>G
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ENSP00000453958.2:p.Pro2198Ala
|
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ENST00000674301.2:c.6592C>G
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ENSP00000501333.2:p.Pro2198Ala
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ENST00000682170.1:n.201C>G
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|
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ENST00000316623.10:c.6592C>G
MANE Select
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ENSP00000325527.5:p.Pro2198Ala
|
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ENST00000674301.1:c.1591C>G
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ENSP00000501333.1:p.Pro531Ala
|
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ENST00000316623.9:c.6592C>G
|
ENSP00000325527.5:p.Pro2198Ala
|
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ENST00000537463.6:c.*2355C>G
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ENSP00000440294.2:n.*2355C>G
|
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ENST00000559133.5:c.1899C>G
|
|
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NM_000138.4:c.6592C>G , LRG_778t1:c.6592C>G
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NP_000129.3:p.Pro2198Ala
|
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NM_000138.5:c.6592C>G
MANE Select
|
NP_000129.3:p.Pro2198Ala
|
|