ENST00000375559.8:c.1007T>A
MANE Select
|
ENSP00000364709.3:p.Met336Lys
|
|
ENST00000375551.7:c.997T>A
|
ENSP00000364701.3:p.Ter333Arg
|
|
ENST00000375559.7:c.1007T>A
|
ENSP00000364709.3:p.Met336Lys
|
|
ENST00000409306.5:c.1003T>A
|
ENSP00000387092.1:p.Ter335Arg
|
|
NM_000504.3:c.1007T>A , LRG_548t1:c.1007T>A
|
NP_000495.1:p.Met336Lys
|
|
NM_001312674.1:c.875T>A
|
NP_001299603.1:p.Met292Lys
|
|
NM_001312675.1:c.997T>A
|
NP_001299604.1:p.Ter333Arg
|
|
NM_000504.4:c.1007T>A
MANE Select
|
NP_000495.1:p.Met336Lys
|
|
NM_001312674.2:c.875T>A
|
NP_001299603.1:p.Met292Lys
|
|
NM_001312675.2:c.997T>A
|
NP_001299604.1:p.Ter333Arg
|
|