ENST00000695651.1:n.1043G=
|
|
|
ENST00000695652.1:c.2572G=
|
ENSP00000512083.1:p.Val858=
|
|
ENST00000695653.1:c.604G=
|
ENSP00000512084.1:p.Val202=
|
|
ENST00000695654.1:c.1819G=
|
ENSP00000512085.1:p.Val607=
|
|
ENST00000695655.1:c.1636G=
|
ENSP00000512086.1:n.1636G=
|
|
ENST00000695692.1:n.2059G=
|
|
|
ENST00000245907.11:c.2695G=
MANE Select
|
ENSP00000245907.4:p.Val899=
|
|
ENST00000245907.10:c.2695G=
|
ENSP00000245907.4:p.Val899=
|
|
ENST00000594005.1:n.271G=
|
|
|
NM_000064.3:c.2695G=
|
NP_000055.2:p.Val899=
|
|
NM_000064.4:c.2695G=
MANE Select
|
NP_000055.2:p.Val899=
|
|