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NM_000138.5:c.7663G>A
MANE Select
|
NP_000129.3:p.Gly2555Arg
|
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ENST00000316623.10:c.7663G>A
MANE Select
|
ENSP00000325527.5:p.Gly2555Arg
|
|
NM_000138.4:c.7663G>A , LRG_778t1:c.7663G>A
|
NP_000129.3:p.Gly2555Arg
|
|
ENST00000316623.9:c.7663G>A
|
ENSP00000325527.5:p.Gly2555Arg
|
|
ENST00000559133.5:c.3032G>A
|
|
|
ENST00000559133.6:c.*471G>A
|
ENSP00000453958.2:n.*471G>A
|
|
ENST00000674301.1:c.2829G>A
|
ENSP00000501333.1:n.2829G>A
|
|
ENST00000674301.2:c.*1176G>A
|
ENSP00000501333.2:n.*1176G>A
|
|
ENST00000682170.1:n.1844G>A
|
|
|
ENST00000682767.1:n.960G>A
|
|