ENST00000649046.1:c.13744C>G
MANE Select
|
ENSP00000496870.1:p.Leu4582Val
|
|
ENST00000649153.1:c.4553C>G
|
|
|
ENST00000650252.1:c.2735C>G
|
ENSP00000496887.1:n.2735C>G
|
|
ENST00000263816.7:c.13744C>G
|
ENSP00000263816.3:p.Leu4582Val
|
|
NM_004525.2:c.13744C>G
|
NP_004516.2:p.Leu4582Val
|
|
XM_011511183.1:c.13615C>G
|
XP_011509485.1:p.Leu4539Val
|
|
XM_011511184.1:c.11455C>G
|
XP_011509486.1:p.Leu3819Val
|
|
NM_004525.3:c.13744C>G
MANE Select
|
NP_004516.2:p.Leu4582Val
|
|
XM_011511183.3:c.13615C>G
|
XP_011509485.1:p.Leu4539Val
|
|
XM_011511184.2:c.11455C>G
|
XP_011509486.1:p.Leu3819Val
|
|