ENST00000695651.1:n.2542C>T
|
|
|
ENST00000695653.1:c.2103C>T
|
ENSP00000512084.1:p.Ala701=
|
|
ENST00000695654.1:c.3219C>T
|
ENSP00000512085.1:p.Ala1073=
|
|
ENST00000695689.1:c.165C>T
|
ENSP00000512101.1:n.165C>T
|
|
ENST00000695690.1:n.385C>T
|
|
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ENST00000695691.1:n.385C>T
|
|
|
ENST00000245907.11:c.4194C>T
MANE Select
|
ENSP00000245907.4:p.Ala1398=
|
|
ENST00000245907.10:c.4194C>T
|
ENSP00000245907.4:p.Ala1398=
|
|
ENST00000596548.1:c.315C>T
|
ENSP00000469744.1:p.Ala105=
|
|
ENST00000599899.5:n.1153C>T
|
|
|
ENST00000601008.1:c.242-4250C>T
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ENSP00000471384.1:n.242-4250C>T
|
|
NM_000064.3:c.4194C>T
|
NP_000055.2:p.Ala1398=
|
|
NM_000064.4:c.4194C>T
MANE Select
|
NP_000055.2:p.Ala1398=
|
|