ENST00000559133.6:c.6937A>G
|
ENSP00000453958.2:p.Ser2313Gly
|
|
ENST00000674301.2:c.*388A>G
|
ENSP00000501333.2:n.*388A>G
|
|
ENST00000682170.1:n.546A>G
|
|
|
ENST00000682767.1:n.172A>G
|
|
|
ENST00000316623.10:c.6937A>G
MANE Select
|
ENSP00000325527.5:p.Ser2313Gly
|
|
ENST00000674301.1:c.2041A>G
|
ENSP00000501333.1:n.2041A>G
|
|
ENST00000316623.9:c.6937A>G
|
ENSP00000325527.5:p.Ser2313Gly
|
|
ENST00000559133.5:c.2244A>G
|
|
|
ENST00000560720.1:n.224A>G
|
|
|
NM_000138.4:c.6937A>G , LRG_778t1:c.6937A>G
|
NP_000129.3:p.Ser2313Gly
|
|
NM_000138.5:c.6937A>G
MANE Select
|
NP_000129.3:p.Ser2313Gly
|
|