ENST00000369538.4:c.441G>T
|
ENSP00000358551.4:p.Met147Ile
|
|
ENST00000520113.7:c.453G>T
MANE Select
|
ENSP00000430075.3:p.Met151Ile
|
|
ENST00000637080.1:c.456G>T
|
ENSP00000489753.1:p.Met152Ile
|
|
ENST00000639077.1:n.118G>T
|
|
|
ENST00000369538.3:c.540G>T
|
ENSP00000358551.3:p.Met180Ile
|
|
ENST00000485564.3:n.327G>T
|
|
|
ENST00000520113.6:c.552G>T
|
ENSP00000430075.2:p.Met184Ile
|
|
NM_000036.2:c.552G>T
|
NP_000027.2:p.Met184Ile
|
|
NM_001172626.1:c.540G>T
|
NP_001166097.1:p.Met180Ile
|
|
NM_000036.3:c.453G>T
MANE Select
|
NP_000027.3:p.Met151Ile
|
|
NM_001172626.2:c.441G>T
|
NP_001166097.2:p.Met147Ile
|
|