ENST00000559133.6:c.6155G=
|
ENSP00000453958.2:p.Arg2052=
|
|
ENST00000674301.2:c.6155G=
|
ENSP00000501333.2:p.Arg2052=
|
|
ENST00000316623.10:c.6155G=
MANE Select
|
ENSP00000325527.5:p.Arg2052=
|
|
ENST00000674301.1:c.1154G=
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ENSP00000501333.1:p.Arg385=
|
|
ENST00000316623.9:c.6155G=
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ENSP00000325527.5:p.Arg2052=
|
|
ENST00000537463.6:c.*1918G=
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ENSP00000440294.2:n.*1918G=
|
|
ENST00000559133.5:c.1462G=
|
|
|
ENST00000560820.1:n.275G=
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|
|
NM_000138.4:c.6155G= , LRG_778t1:c.6155G=
|
NP_000129.3:p.Arg2052=
|
|
NM_000138.5:c.6155G=
MANE Select
|
NP_000129.3:p.Arg2052=
|
|