NM_000791.4:c.231C>T
MANE Select
|
NP_000782.1:p.Ser77=
|
ENST00000439211.7:c.231C>T
MANE Select
|
ENSP00000396308.2:p.Ser77=
|
NM_000791.3:c.231C>T
|
NP_000782.1:p.Ser77=
|
NM_001290354.1:c.75C>T
|
NP_001277283.1:p.Ser25=
|
NM_001290354.2:c.75C>T
|
NP_001277283.1:p.Ser25=
|
NM_001290357.1:c.231C>T
|
NP_001277286.1:p.Ser77=
|
NM_001290357.2:c.231C>T
|
NP_001277286.1:p.Ser77=
|
NR_110936.1:n.673C>T
|
|
NR_110936.2:n.675C>T
|
|
ENST00000439211.6:c.231C>T
|
ENSP00000396308.2:p.Ser77=
|
ENST00000504396.1:c.75C>T
|
ENSP00000421334.1:p.Ser25=
|
ENST00000505337.5:c.231C>T
|
ENSP00000426474.1:p.Ser77=
|
ENST00000508282.1:n.189C>T
|
|
ENST00000511032.5:c.231C>T
|
ENSP00000422732.1:p.Ser77=
|
ENST00000513048.5:n.239C>T
|
|
ENST00000513314.1:n.123C>T
|
|