ENST00000369538.4:c.1304T>A
|
ENSP00000358551.4:p.Leu435His
|
|
ENST00000520113.7:c.1316T>A
MANE Select
|
ENSP00000430075.3:p.Leu439His
|
|
ENST00000637080.1:c.1099T>A
|
ENSP00000489753.1:n.1099T>A
|
|
ENST00000639077.1:n.981T>A
|
|
|
ENST00000369538.3:c.1403T>A
|
ENSP00000358551.3:p.Leu468His
|
|
ENST00000520113.6:c.1415T>A
|
ENSP00000430075.2:p.Leu472His
|
|
NM_000036.2:c.1415T>A
|
NP_000027.2:p.Leu472His
|
|
NM_001172626.1:c.1403T>A
|
NP_001166097.1:p.Leu468His
|
|
NM_000036.3:c.1316T>A
MANE Select
|
NP_000027.3:p.Leu439His
|
|
NM_001172626.2:c.1304T>A
|
NP_001166097.2:p.Leu435His
|
|