ENST00000559133.6:c.6962G>T
|
ENSP00000453958.2:p.Gly2321Val
|
|
ENST00000674301.2:c.*413G>T
|
ENSP00000501333.2:n.*413G>T
|
|
ENST00000682170.1:n.571G>T
|
|
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ENST00000682767.1:n.197G>T
|
|
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ENST00000316623.10:c.6962G>T
MANE Select
|
ENSP00000325527.5:p.Gly2321Val
|
|
ENST00000674301.1:c.2066G>T
|
ENSP00000501333.1:n.2066G>T
|
|
ENST00000316623.9:c.6962G>T
|
ENSP00000325527.5:p.Gly2321Val
|
|
ENST00000559133.5:c.2269G>T
|
|
|
ENST00000560720.1:n.249G>T
|
|
|
NM_000138.4:c.6962G>T , LRG_778t1:c.6962G>T
|
NP_000129.3:p.Gly2321Val
|
|
NM_000138.5:c.6962G>T
MANE Select
|
NP_000129.3:p.Gly2321Val
|
|