ENST00000205402.10:c.1056C>A
MANE Select
|
ENSP00000205402.3:p.Ala352=
|
|
ENST00000205402.9:c.1056C>A
|
ENSP00000205402.3:p.Ala352=
|
|
ENST00000415325.5:c.*730C>A
|
ENSP00000402593.1:n.*730C>A
|
|
ENST00000417551.5:c.1056C>A
|
ENSP00000390667.1:p.Ala352=
|
|
ENST00000437604.6:c.912C>A
|
ENSP00000387542.2:p.Ala304=
|
|
ENST00000440410.5:c.987C>A
|
ENSP00000417016.1:p.Ala329=
|
|
NM_000108.4:c.1056C>A
|
NP_000099.2:p.Ala352=
|
|
NM_001289750.1:c.759C>A
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NP_001276679.1:p.Ala253=
|
|
NM_001289751.1:c.987C>A
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NP_001276680.1:p.Ala329=
|
|
NM_001289752.1:c.912C>A
|
NP_001276681.1:p.Ala304=
|
|
NM_000108.5:c.1056C>A
MANE Select
|
NP_000099.2:p.Ala352=
|
|