ENST00000369538.4:c.1237G>T
|
ENSP00000358551.4:p.Ala413Ser
|
|
ENST00000520113.7:c.1249G>T
MANE Select
|
ENSP00000430075.3:p.Ala417Ser
|
|
ENST00000637080.1:c.1032G>T
|
ENSP00000489753.1:n.1032G>T
|
|
ENST00000639077.1:n.914G>T
|
|
|
ENST00000369538.3:c.1336G>T
|
ENSP00000358551.3:p.Ala446Ser
|
|
ENST00000520113.6:c.1348G>T
|
ENSP00000430075.2:p.Ala450Ser
|
|
NM_000036.2:c.1348G>T
|
NP_000027.2:p.Ala450Ser
|
|
NM_001172626.1:c.1336G>T
|
NP_001166097.1:p.Ala446Ser
|
|
NM_000036.3:c.1249G>T
MANE Select
|
NP_000027.3:p.Ala417Ser
|
|
NM_001172626.2:c.1237G>T
|
NP_001166097.2:p.Ala413Ser
|
|