ENST00000559133.6:c.6968C>G
|
ENSP00000453958.2:p.Thr2323Ser
|
|
ENST00000674301.2:c.*419C>G
|
ENSP00000501333.2:n.*419C>G
|
|
ENST00000682170.1:n.577C>G
|
|
|
ENST00000682767.1:n.203C>G
|
|
|
ENST00000316623.10:c.6968C>G
MANE Select
|
ENSP00000325527.5:p.Thr2323Ser
|
|
ENST00000674301.1:c.2072C>G
|
ENSP00000501333.1:n.2072C>G
|
|
ENST00000316623.9:c.6968C>G
|
ENSP00000325527.5:p.Thr2323Ser
|
|
ENST00000559133.5:c.2275C>G
|
|
|
ENST00000560720.1:n.255C>G
|
|
|
NM_000138.4:c.6968C>G , LRG_778t1:c.6968C>G
|
NP_000129.3:p.Thr2323Ser
|
|
NM_000138.5:c.6968C>G
MANE Select
|
NP_000129.3:p.Thr2323Ser
|
|