ENST00000601549.2:n.459C>T
|
|
|
ENST00000648053.1:n.269C>T
|
|
|
ENST00000648319.1:c.837C>T
MANE Select
|
ENSP00000496939.1:p.Ala279=
|
|
ENST00000262888.7:c.837C>T
|
ENSP00000262888.3:p.Ala279=
|
|
ENST00000598836.1:c.16C>T
|
|
|
ENST00000599720.5:c.*107C>T
|
ENSP00000472513.1:n.*107C>T
|
|
ENST00000600408.1:c.126C>T
|
ENSP00000472510.1:p.Ala42=
|
|
ENST00000601549.1:n.146C>T
|
|
|
ENST00000615047.4:c.441C>T
|
ENSP00000485014.1:p.Ala147=
|
|
NM_002250.2:c.837C>T
|
NP_002241.1:p.Ala279=
|
|
XM_005258882.2:c.741C>T
|
XP_005258939.1:p.Ala247=
|
|
XM_005258883.2:c.648C>T
|
XP_005258940.1:p.Ala216=
|
|
XR_935823.1:n.2083C>T
|
|
|
XR_002958313.1:n.2229C>T
|
|
|
NM_002250.3:c.837C>T
MANE Select
|
NP_002241.1:p.Ala279=
|
|