ENST00000649046.1:c.10195C>T
MANE Select
|
ENSP00000496870.1:p.Arg3399Ter
|
|
ENST00000649153.1:c.1095C>T
|
|
|
ENST00000263816.7:c.10195C>T
|
ENSP00000263816.3:p.Arg3399Ter
|
|
ENST00000461418.1:n.396C>T
|
|
|
NM_004525.2:c.10195C>T
|
NP_004516.2:p.Arg3399Ter
|
|
XM_011511183.1:c.10195C>T
|
XP_011509485.1:p.Arg3399Ter
|
|
XM_011511184.1:c.7906C>T
|
XP_011509486.1:p.Arg2636Ter
|
|
NM_004525.3:c.10195C>T
MANE Select
|
NP_004516.2:p.Arg3399Ter
|
|
XM_011511183.3:c.10195C>T
|
XP_011509485.1:p.Arg3399Ter
|
|
XM_011511184.2:c.7906C>T
|
XP_011509486.1:p.Arg2636Ter
|
|