ENST00000695651.1:n.2890T>C
|
|
|
ENST00000695653.1:c.2451T>C
|
ENSP00000512084.1:p.Ala817=
|
|
ENST00000695654.1:c.3567T>C
|
ENSP00000512085.1:p.Ala1189=
|
|
ENST00000695689.1:c.513T>C
|
ENSP00000512101.1:n.513T>C
|
|
ENST00000695690.1:n.1607T>C
|
|
|
ENST00000695691.1:n.1403T>C
|
|
|
ENST00000245907.11:c.4542T>C
MANE Select
|
ENSP00000245907.4:p.Ala1514=
|
|
ENST00000245907.10:c.4542T>C
|
ENSP00000245907.4:p.Ala1514=
|
|
ENST00000599668.1:n.137T>C
|
|
|
ENST00000599899.5:n.1501T>C
|
|
|
ENST00000601008.1:c.242-1453T>C
|
ENSP00000471384.1:n.242-1453T>C
|
|
NM_000064.3:c.4542T>C
|
NP_000055.2:p.Ala1514=
|
|
NM_000064.4:c.4542T>C
MANE Select
|
NP_000055.2:p.Ala1514=
|
|