ENST00000649046.1:c.13747T>G
MANE Select
|
ENSP00000496870.1:p.Phe4583Val
|
|
ENST00000649153.1:c.4556T>G
|
|
|
ENST00000650252.1:c.2738T>G
|
ENSP00000496887.1:n.2738T>G
|
|
ENST00000263816.7:c.13747T>G
|
ENSP00000263816.3:p.Phe4583Val
|
|
NM_004525.2:c.13747T>G
|
NP_004516.2:p.Phe4583Val
|
|
XM_011511183.1:c.13618T>G
|
XP_011509485.1:p.Phe4540Val
|
|
XM_011511184.1:c.11458T>G
|
XP_011509486.1:p.Phe3820Val
|
|
NM_004525.3:c.13747T>G
MANE Select
|
NP_004516.2:p.Phe4583Val
|
|
XM_011511183.3:c.13618T>G
|
XP_011509485.1:p.Phe4540Val
|
|
XM_011511184.2:c.11458T>G
|
XP_011509486.1:p.Phe3820Val
|
|