ENST00000649046.1:c.12252C=
MANE Select
|
ENSP00000496870.1:p.Ile4084=
|
|
ENST00000649153.1:c.3152C=
|
|
|
ENST00000650252.1:c.1280C=
|
ENSP00000496887.1:p.Ser427=
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|
ENST00000263816.7:c.12252C=
|
ENSP00000263816.3:p.Ile4084=
|
|
NM_004525.2:c.12252C=
|
NP_004516.2:p.Ile4084=
|
|
XM_011511183.1:c.12123C=
|
XP_011509485.1:p.Ile4041=
|
|
XM_011511184.1:c.9963C=
|
XP_011509486.1:p.Ile3321=
|
|
NM_004525.3:c.12252C=
MANE Select
|
NP_004516.2:p.Ile4084=
|
|
XM_011511183.3:c.12123C=
|
XP_011509485.1:p.Ile4041=
|
|
XM_011511184.2:c.9963C=
|
XP_011509486.1:p.Ile3321=
|
|