ENST00000649046.1:c.12266A>G
MANE Select
|
ENSP00000496870.1:p.Tyr4089Cys
|
|
ENST00000649153.1:c.3166A>G
|
|
|
ENST00000650252.1:c.1294A>G
|
ENSP00000496887.1:p.Met432Val
|
|
ENST00000263816.7:c.12266A>G
|
ENSP00000263816.3:p.Tyr4089Cys
|
|
NM_004525.2:c.12266A>G
|
NP_004516.2:p.Tyr4089Cys
|
|
XM_011511183.1:c.12137A>G
|
XP_011509485.1:p.Tyr4046Cys
|
|
XM_011511184.1:c.9977A>G
|
XP_011509486.1:p.Tyr3326Cys
|
|
NM_004525.3:c.12266A>G
MANE Select
|
NP_004516.2:p.Tyr4089Cys
|
|
XM_011511183.3:c.12137A>G
|
XP_011509485.1:p.Tyr4046Cys
|
|
XM_011511184.2:c.9977A>G
|
XP_011509486.1:p.Tyr3326Cys
|
|