ENST00000649046.1:c.13746C>T
MANE Select
|
ENSP00000496870.1:p.Leu4582=
|
|
ENST00000649153.1:c.4555C>T
|
|
|
ENST00000650252.1:c.2737C>T
|
ENSP00000496887.1:n.2737C>T
|
|
ENST00000263816.7:c.13746C>T
|
ENSP00000263816.3:p.Leu4582=
|
|
NM_004525.2:c.13746C>T
|
NP_004516.2:p.Leu4582=
|
|
XM_011511183.1:c.13617C>T
|
XP_011509485.1:p.Leu4539=
|
|
XM_011511184.1:c.11457C>T
|
XP_011509486.1:p.Leu3819=
|
|
NM_004525.3:c.13746C>T
MANE Select
|
NP_004516.2:p.Leu4582=
|
|
XM_011511183.3:c.13617C>T
|
XP_011509485.1:p.Leu4539=
|
|
XM_011511184.2:c.11457C>T
|
XP_011509486.1:p.Leu3819=
|
|