ENST00000682422.1:n.859C>G
|
|
|
ENST00000682545.1:c.*284C>G
|
ENSP00000508402.1:n.*284C>G
|
|
ENST00000682887.1:c.1679C>G
|
ENSP00000506946.1:n.1679C>G
|
|
ENST00000683302.1:c.1209C>G
|
ENSP00000507885.1:p.Ala403=
|
|
ENST00000683557.1:c.*110C>G
|
ENSP00000508029.1:n.*110C>G
|
|
ENST00000367282.6:c.1278C>G
MANE Select
|
ENSP00000356251.4:p.Ala426=
|
|
ENST00000367282.5:c.1278C>G
|
ENSP00000356251.4:p.Ala426=
|
|
NM_004767.3:c.1278C>G
|
NP_004758.3:p.Ala426=
|
|
XM_011510158.1:c.717C>G
|
XP_011508460.1:p.Ala239=
|
|
NM_004767.4:c.1278C>G
|
NP_004758.3:p.Ala426=
|
|
XM_011510158.2:c.717C>G
|
XP_011508460.1:p.Ala239=
|
|
NM_004767.5:c.1278C>G
MANE Select
|
NP_004758.3:p.Ala426=
|
|