ENST00000545712.7:c.729A>T
MANE Select
|
ENSP00000445920.1:p.Pro243=
|
|
ENST00000537496.5:c.*294A>T
|
ENSP00000444793.1:n.*294A>T
|
|
ENST00000540016.5:c.573A>T
|
ENSP00000474582.1:p.Pro191=
|
|
ENST00000541763.6:c.954A>T
|
ENSP00000474981.1:n.954A>T
|
|
ENST00000544051.5:c.*610A>T
|
ENSP00000438079.1:n.*610A>T
|
|
ENST00000545712.6:c.729A>T
|
ENSP00000445920.1:p.Pro243=
|
|
NM_052845.3:c.729A>T
|
NP_443077.1:p.Pro243=
|
|
NR_038118.1:n.889A>T
|
|
|
XM_011538266.1:c.*76A>T
|
XP_011536568.1:n.*76A>T
|
|
XM_011538267.1:c.*76A>T
|
XP_011536569.1:n.*76A>T
|
|
XM_011538268.1:c.456A>T
|
XP_011536570.1:p.Pro152=
|
|
XM_011538269.1:c.453A>T
|
XP_011536571.1:p.Pro151=
|
|
XM_011538267.3:c.*76A>T
|
XP_011536569.1:n.*76A>T
|
|
XM_011538268.2:c.456A>T
|
XP_011536570.1:p.Pro152=
|
|
XM_011538269.2:c.453A>T
|
XP_011536571.1:p.Pro151=
|
|
NM_052845.4:c.729A>T
MANE Select
|
NP_443077.1:p.Pro243=
|
|
NR_038118.2:n.840A>T
|
|
|