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NM_000138.5:c.6728G>A
MANE Select
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NP_000129.3:p.Arg2243Lys
|
|
ENST00000316623.10:c.6728G>A
MANE Select
|
ENSP00000325527.5:p.Arg2243Lys
|
|
NM_000138.4:c.6728G>A , LRG_778t1:c.6728G>A
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NP_000129.3:p.Arg2243Lys
|
|
ENST00000316623.9:c.6728G>A
|
ENSP00000325527.5:p.Arg2243Lys
|
|
ENST00000537463.6:c.*2491G>A
|
ENSP00000440294.2:n.*2491G>A
|
|
ENST00000559133.5:c.2035G>A
|
|
|
ENST00000559133.6:c.6728G>A
|
ENSP00000453958.2:p.Arg2243Lys
|
|
ENST00000560720.1:n.15G>A
|
|
|
ENST00000674301.1:c.1832G>A
|
ENSP00000501333.1:n.1832G>A
|
|
ENST00000674301.2:c.*179G>A
|
ENSP00000501333.2:n.*179G>A
|
|
ENST00000682170.1:n.337G>A
|
|