ENST00000369538.4:c.463C>G
|
ENSP00000358551.4:p.Pro155Ala
|
|
ENST00000520113.7:c.475C>G
MANE Select
|
ENSP00000430075.3:p.Pro159Ala
|
|
ENST00000637080.1:c.478C>G
|
ENSP00000489753.1:p.Pro160Ala
|
|
ENST00000639077.1:n.140C>G
|
|
|
ENST00000369538.3:c.562C>G
|
ENSP00000358551.3:p.Pro188Ala
|
|
ENST00000485564.3:n.349C>G
|
|
|
ENST00000520113.6:c.574C>G
|
ENSP00000430075.2:p.Pro192Ala
|
|
NM_000036.2:c.574C>G
|
NP_000027.2:p.Pro192Ala
|
|
NM_001172626.1:c.562C>G
|
NP_001166097.1:p.Pro188Ala
|
|
NM_000036.3:c.475C>G
MANE Select
|
NP_000027.3:p.Pro159Ala
|
|
NM_001172626.2:c.463C>G
|
NP_001166097.2:p.Pro155Ala
|
|