ENST00000355832.10:c.3522G>T
MANE Select
|
ENSP00000348089.5:p.Met1174Ile
|
|
ENST00000679552.1:n.593G>T
|
|
|
ENST00000679871.1:n.668G>T
|
|
|
ENST00000679974.1:n.571G>T
|
|
|
ENST00000681632.1:n.4925G>T
|
|
|
ENST00000681659.1:c.3363G>T
|
ENSP00000505631.1:p.Met1121Ile
|
|
ENST00000355832.9:c.3522G>T
|
ENSP00000348089.5:p.Met1174Ile
|
|
ENST00000623073.3:c.*1818G>T
|
ENSP00000485650.1:n.*1818G>T
|
|
ENST00000623115.3:c.1632G>T
|
ENSP00000485321.1:p.Met544Ile
|
|
ENST00000624341.3:c.1354G>T
|
|
|
NM_000124.3:c.3522G>T
|
NP_000115.1:p.Met1174Ile
|
|
XR_945953.1:n.243-1127C>A
|
|
|
NM_001346440.1:c.3522G>T
|
NP_001333369.1:p.Met1174Ile
|
|
NM_000124.4:c.3522G>T
MANE Select
|
NP_000115.1:p.Met1174Ile
|
|
NM_001346440.2:c.3522G>T
|
NP_001333369.1:p.Met1174Ile
|
|