ENST00000369538.4:c.535G>T
|
ENSP00000358551.4:p.Val179Phe
|
|
ENST00000520113.7:c.547G>T
MANE Select
|
ENSP00000430075.3:p.Val183Phe
|
|
ENST00000637080.1:c.550G>T
|
ENSP00000489753.1:p.Val184Leu
|
|
ENST00000639077.1:n.212G>T
|
|
|
ENST00000369538.3:c.634G>T
|
ENSP00000358551.3:p.Val212Phe
|
|
ENST00000485564.3:n.421G>T
|
|
|
ENST00000520113.6:c.646G>T
|
ENSP00000430075.2:p.Val216Phe
|
|
NM_000036.2:c.646G>T
|
NP_000027.2:p.Val216Phe
|
|
NM_001172626.1:c.634G>T
|
NP_001166097.1:p.Val212Phe
|
|
NM_000036.3:c.547G>T
MANE Select
|
NP_000027.3:p.Val183Phe
|
|
NM_001172626.2:c.535G>T
|
NP_001166097.2:p.Val179Phe
|
|