ENST00000328300.11:c.4177A>T
MANE Select
|
ENSP00000331902.7:p.Lys1393Ter
|
|
ENST00000361603.7:c.4159A>T
|
ENSP00000354505.2:p.Lys1387Ter
|
|
ENST00000510690.2:n.671A>T
|
|
|
ENST00000328300.10:c.4177A>T
|
ENSP00000331902.6:p.Lys1393Ter
|
|
ENST00000361603.6:c.4159A>T
|
ENSP00000354505.2:p.Lys1387Ter
|
|
ENST00000489230.1:n.580A>T
|
|
|
NM_000495.4:c.4159A>T
|
NP_000486.1:p.Lys1387Ter
|
|
NM_033380.2:c.4177A>T
|
NP_203699.1:p.Lys1393Ter
|
|
XM_005262070.2:c.4168A>T
|
XP_005262127.1:p.Lys1390Ter
|
|
XM_006724616.2:c.4177A>T
|
XP_006724679.1:p.Lys1393Ter
|
|
XM_011530849.1:c.3853A>T
|
XP_011529151.1:p.Lys1285Ter
|
|
XM_011530851.1:c.1750A>T
|
XP_011529153.1:p.Lys584Ter
|
|
XM_011530849.2:c.4192A>T
|
XP_011529151.2:p.Lys1398Ter
|
|
XM_017029259.2:c.4183A>T
|
XP_016884748.1:p.Lys1395Ter
|
|
XM_017029260.1:c.4174A>T
|
XP_016884749.1:p.Lys1392Ter
|
|
XM_017029263.2:c.2512A>T
|
XP_016884752.1:p.Lys838Ter
|
|
NM_000495.5:c.4159A>T
|
NP_000486.1:p.Lys1387Ter
|
|
NM_033380.3:c.4177A>T
MANE Select
|
NP_203699.1:p.Lys1393Ter
|
|