ENST00000307998.11:c.192C>T
MANE Select
|
ENSP00000309953.6:p.Ala64=
|
|
ENST00000307998.10:c.192C>T
|
ENSP00000309953.6:p.Ala64=
|
|
ENST00000526624.5:c.192C>T
|
ENSP00000435419.1:p.Ala64=
|
|
ENST00000527378.1:c.192C>T
|
ENSP00000435963.1:p.Ala64=
|
|
ENST00000528176.5:c.192C>T
|
ENSP00000434151.1:p.Ala64=
|
|
ENST00000530850.1:c.*4C>T
|
ENSP00000437238.1:n.*4C>T
|
|
ENST00000531005.5:n.688C>T
|
|
|
ENST00000531972.5:c.192C>T
|
ENSP00000435295.1:p.Ala64=
|
|
ENST00000533347.5:c.*4C>T
|
ENSP00000435823.1:n.*4C>T
|
|
NM_016938.4:c.192C>T
|
NP_058634.4:p.Ala64=
|
|
NR_037718.1:n.451C>T
|
|
|
NM_016938.5:c.192C>T
MANE Select
|
NP_058634.4:p.Ala64=
|
|
NR_037718.2:n.317C>T
|
|
|