ENST00000695651.1:n.1084C>G
|
|
|
ENST00000695652.1:c.2613C>G
|
ENSP00000512083.1:p.Val871=
|
|
ENST00000695653.1:c.645C>G
|
ENSP00000512084.1:p.Val215=
|
|
ENST00000695654.1:c.1860C>G
|
ENSP00000512085.1:p.Val620=
|
|
ENST00000695655.1:c.1677C>G
|
ENSP00000512086.1:n.1677C>G
|
|
ENST00000695692.1:n.2100C>G
|
|
|
ENST00000245907.11:c.2736C>G
MANE Select
|
ENSP00000245907.4:p.Val912=
|
|
ENST00000245907.10:c.2736C>G
|
ENSP00000245907.4:p.Val912=
|
|
ENST00000594005.1:n.312C>G
|
|
|
NM_000064.3:c.2736C>G
|
NP_000055.2:p.Val912=
|
|
NM_000064.4:c.2736C>G
MANE Select
|
NP_000055.2:p.Val912=
|
|