ENST00000559133.6:c.5992T>G
|
ENSP00000453958.2:p.Cys1998Gly
|
|
ENST00000674301.2:c.5992T>G
|
ENSP00000501333.2:p.Cys1998Gly
|
|
ENST00000684448.1:n.4666T>G
|
|
|
ENST00000316623.10:c.5992T>G
MANE Select
|
ENSP00000325527.5:p.Cys1998Gly
|
|
ENST00000674301.1:c.991T>G
|
ENSP00000501333.1:p.Cys331Gly
|
|
ENST00000316623.9:c.5992T>G
|
ENSP00000325527.5:p.Cys1998Gly
|
|
ENST00000537463.6:c.*1755T>G
|
ENSP00000440294.2:n.*1755T>G
|
|
ENST00000559133.5:c.1299T>G
|
|
|
ENST00000560820.1:n.112T>G
|
|
|
NM_000138.4:c.5992T>G , LRG_778t1:c.5992T>G
|
NP_000129.3:p.Cys1998Gly
|
|
NM_000138.5:c.5992T>G
MANE Select
|
NP_000129.3:p.Cys1998Gly
|
|