ENST00000649046.1:c.12159T>G
MANE Select
|
ENSP00000496870.1:p.Ser4053=
|
|
ENST00000649153.1:c.3059T>G
|
|
|
ENST00000650252.1:c.1187T>G
|
ENSP00000496887.1:p.Leu396Arg
|
|
ENST00000263816.7:c.12159T>G
|
ENSP00000263816.3:p.Ser4053=
|
|
NM_004525.2:c.12159T>G
|
NP_004516.2:p.Ser4053=
|
|
XM_011511183.1:c.12030T>G
|
XP_011509485.1:p.Ser4010=
|
|
XM_011511184.1:c.9870T>G
|
XP_011509486.1:p.Ser3290=
|
|
NM_004525.3:c.12159T>G
MANE Select
|
NP_004516.2:p.Ser4053=
|
|
XM_011511183.3:c.12030T>G
|
XP_011509485.1:p.Ser4010=
|
|
XM_011511184.2:c.9870T>G
|
XP_011509486.1:p.Ser3290=
|
|