ENST00000695651.1:n.2044C>G
|
|
|
ENST00000695652.1:c.3573C>G
|
ENSP00000512083.1:p.Ala1191=
|
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ENST00000695653.1:c.1605C>G
|
ENSP00000512084.1:p.Ala535=
|
|
ENST00000695654.1:c.2721C>G
|
ENSP00000512085.1:p.Ala907=
|
|
ENST00000695655.1:c.2637C>G
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ENSP00000512086.1:n.2637C>G
|
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ENST00000695692.1:n.3060C>G
|
|
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ENST00000245907.11:c.3696C>G
MANE Select
|
ENSP00000245907.4:p.Ala1232=
|
|
ENST00000245907.10:c.3696C>G
|
ENSP00000245907.4:p.Ala1232=
|
|
ENST00000596238.1:n.139C>G
|
|
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ENST00000601008.1:c.241+508C>G
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ENSP00000471384.1:n.241+508C>G
|
|
NM_000064.3:c.3696C>G
|
NP_000055.2:p.Ala1232=
|
|
NM_000064.4:c.3696C>G
MANE Select
|
NP_000055.2:p.Ala1232=
|
|