ENST00000649046.1:c.13753C>A
MANE Select
|
ENSP00000496870.1:p.Arg4585=
|
|
ENST00000649153.1:c.4562C>A
|
|
|
ENST00000650252.1:c.2744C>A
|
ENSP00000496887.1:n.2744C>A
|
|
ENST00000263816.7:c.13753C>A
|
ENSP00000263816.3:p.Arg4585=
|
|
NM_004525.2:c.13753C>A
|
NP_004516.2:p.Arg4585=
|
|
XM_011511183.1:c.13624C>A
|
XP_011509485.1:p.Arg4542=
|
|
XM_011511184.1:c.11464C>A
|
XP_011509486.1:p.Arg3822=
|
|
NM_004525.3:c.13753C>A
MANE Select
|
NP_004516.2:p.Arg4585=
|
|
XM_011511183.3:c.13624C>A
|
XP_011509485.1:p.Arg4542=
|
|
XM_011511184.2:c.11464C>A
|
XP_011509486.1:p.Arg3822=
|
|