ENST00000369538.4:c.1251T>G
|
ENSP00000358551.4:p.His417Gln
|
|
ENST00000520113.7:c.1263T>G
MANE Select
|
ENSP00000430075.3:p.His421Gln
|
|
ENST00000637080.1:c.1046T>G
|
ENSP00000489753.1:n.1046T>G
|
|
ENST00000639077.1:n.928T>G
|
|
|
ENST00000369538.3:c.1350T>G
|
ENSP00000358551.3:p.His450Gln
|
|
ENST00000520113.6:c.1362T>G
|
ENSP00000430075.2:p.His454Gln
|
|
NM_000036.2:c.1362T>G
|
NP_000027.2:p.His454Gln
|
|
NM_001172626.1:c.1350T>G
|
NP_001166097.1:p.His450Gln
|
|
NM_000036.3:c.1263T>G
MANE Select
|
NP_000027.3:p.His421Gln
|
|
NM_001172626.2:c.1251T>G
|
NP_001166097.2:p.His417Gln
|
|