ENST00000649046.1:c.12226G>T
MANE Select
|
ENSP00000496870.1:p.Glu4076Ter
|
|
ENST00000649153.1:c.3126G>T
|
|
|
ENST00000650252.1:c.1254G>T
|
ENSP00000496887.1:p.Gln418His
|
|
ENST00000263816.7:c.12226G>T
|
ENSP00000263816.3:p.Glu4076Ter
|
|
NM_004525.2:c.12226G>T
|
NP_004516.2:p.Glu4076Ter
|
|
XM_011511183.1:c.12097G>T
|
XP_011509485.1:p.Glu4033Ter
|
|
XM_011511184.1:c.9937G>T
|
XP_011509486.1:p.Glu3313Ter
|
|
NM_004525.3:c.12226G>T
MANE Select
|
NP_004516.2:p.Glu4076Ter
|
|
XM_011511183.3:c.12097G>T
|
XP_011509485.1:p.Glu4033Ter
|
|
XM_011511184.2:c.9937G>T
|
XP_011509486.1:p.Glu3313Ter
|
|