ENST00000649046.1:c.12195A>G
MANE Select
|
ENSP00000496870.1:p.Arg4065=
|
|
ENST00000649153.1:c.3095A>G
|
|
|
ENST00000650252.1:c.1223A>G
|
ENSP00000496887.1:p.Glu408Gly
|
|
ENST00000263816.7:c.12195A>G
|
ENSP00000263816.3:p.Arg4065=
|
|
NM_004525.2:c.12195A>G
|
NP_004516.2:p.Arg4065=
|
|
XM_011511183.1:c.12066A>G
|
XP_011509485.1:p.Arg4022=
|
|
XM_011511184.1:c.9906A>G
|
XP_011509486.1:p.Arg3302=
|
|
NM_004525.3:c.12195A>G
MANE Select
|
NP_004516.2:p.Arg4065=
|
|
XM_011511183.3:c.12066A>G
|
XP_011509485.1:p.Arg4022=
|
|
XM_011511184.2:c.9906A>G
|
XP_011509486.1:p.Arg3302=
|
|