ENST00000205402.10:c.1038A>G
MANE Select
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ENSP00000205402.3:p.Lys346=
|
|
ENST00000205402.9:c.1038A>G
|
ENSP00000205402.3:p.Lys346=
|
|
ENST00000415325.5:c.*712A>G
|
ENSP00000402593.1:n.*712A>G
|
|
ENST00000417551.5:c.1038A>G
|
ENSP00000390667.1:p.Lys346=
|
|
ENST00000437604.6:c.894A>G
|
ENSP00000387542.2:p.Lys298=
|
|
ENST00000440410.5:c.969A>G
|
ENSP00000417016.1:p.Lys323=
|
|
NM_000108.4:c.1038A>G
|
NP_000099.2:p.Lys346=
|
|
NM_001289750.1:c.741A>G
|
NP_001276679.1:p.Lys247=
|
|
NM_001289751.1:c.969A>G
|
NP_001276680.1:p.Lys323=
|
|
NM_001289752.1:c.894A>G
|
NP_001276681.1:p.Lys298=
|
|
NM_000108.5:c.1038A>G
MANE Select
|
NP_000099.2:p.Lys346=
|
|