ENST00000369538.4:c.409T>C
|
ENSP00000358551.4:p.Tyr137His
|
|
ENST00000520113.7:c.421T>C
MANE Select
|
ENSP00000430075.3:p.Tyr141His
|
|
ENST00000637080.1:c.424T>C
|
ENSP00000489753.1:p.Tyr142His
|
|
ENST00000639077.1:n.86T>C
|
|
|
ENST00000369538.3:c.508T>C
|
ENSP00000358551.3:p.Tyr170His
|
|
ENST00000485564.3:n.295T>C
|
|
|
ENST00000520113.6:c.520T>C
|
ENSP00000430075.2:p.Tyr174His
|
|
NM_000036.2:c.520T>C
|
NP_000027.2:p.Tyr174His
|
|
NM_001172626.1:c.508T>C
|
NP_001166097.1:p.Tyr170His
|
|
NM_000036.3:c.421T>C
MANE Select
|
NP_000027.3:p.Tyr141His
|
|
NM_001172626.2:c.409T>C
|
NP_001166097.2:p.Tyr137His
|
|