ENST00000649046.1:c.12192T>C
MANE Select
|
ENSP00000496870.1:p.Ile4064=
|
|
ENST00000649153.1:c.3092T>C
|
|
|
ENST00000650252.1:c.1220T>C
|
ENSP00000496887.1:p.Phe407Ser
|
|
ENST00000263816.7:c.12192T>C
|
ENSP00000263816.3:p.Ile4064=
|
|
NM_004525.2:c.12192T>C
|
NP_004516.2:p.Ile4064=
|
|
XM_011511183.1:c.12063T>C
|
XP_011509485.1:p.Ile4021=
|
|
XM_011511184.1:c.9903T>C
|
XP_011509486.1:p.Ile3301=
|
|
NM_004525.3:c.12192T>C
MANE Select
|
NP_004516.2:p.Ile4064=
|
|
XM_011511183.3:c.12063T>C
|
XP_011509485.1:p.Ile4021=
|
|
XM_011511184.2:c.9903T>C
|
XP_011509486.1:p.Ile3301=
|
|