ENST00000559133.6:c.*1122A>G
|
ENSP00000453958.2:n.*1122A>G
|
|
ENST00000674301.2:c.*1827A>G
|
ENSP00000501333.2:n.*1827A>G
|
|
ENST00000682158.1:n.1695A>G
|
|
|
ENST00000682170.1:n.2495A>G
|
|
|
ENST00000682767.1:n.1611A>G
|
|
|
ENST00000316623.10:c.8314A>G
MANE Select
|
ENSP00000325527.5:p.Ser2772Gly
|
|
ENST00000674301.1:c.3480A>G
|
ENSP00000501333.1:n.3480A>G
|
|
ENST00000316623.9:c.8314A>G
|
ENSP00000325527.5:p.Ser2772Gly
|
|
ENST00000559133.5:c.3683A>G
|
|
|
ENST00000561429.1:n.569A>G
|
|
|
NM_000138.4:c.8314A>G , LRG_778t1:c.8314A>G
|
NP_000129.3:p.Ser2772Gly
|
|
NM_000138.5:c.8314A>G
MANE Select
|
NP_000129.3:p.Ser2772Gly
|
|