ENST00000369538.4:c.505G>T
|
ENSP00000358551.4:p.Ala169Ser
|
|
ENST00000520113.7:c.517G>T
MANE Select
|
ENSP00000430075.3:p.Ala173Ser
|
|
ENST00000637080.1:c.520G>T
|
ENSP00000489753.1:p.Ala174Ser
|
|
ENST00000639077.1:n.182G>T
|
|
|
ENST00000369538.3:c.604G>T
|
ENSP00000358551.3:p.Ala202Ser
|
|
ENST00000485564.3:n.391G>T
|
|
|
ENST00000520113.6:c.616G>T
|
ENSP00000430075.2:p.Ala206Ser
|
|
NM_000036.2:c.616G>T
|
NP_000027.2:p.Ala206Ser
|
|
NM_001172626.1:c.604G>T
|
NP_001166097.1:p.Ala202Ser
|
|
NM_000036.3:c.517G>T
MANE Select
|
NP_000027.3:p.Ala173Ser
|
|
NM_001172626.2:c.505G>T
|
NP_001166097.2:p.Ala169Ser
|
|