ENST00000695651.1:n.1044T>C
|
|
|
ENST00000695652.1:c.2573T>C
|
ENSP00000512083.1:p.Val858Ala
|
|
ENST00000695653.1:c.605T>C
|
ENSP00000512084.1:p.Val202Ala
|
|
ENST00000695654.1:c.1820T>C
|
ENSP00000512085.1:p.Val607Ala
|
|
ENST00000695655.1:c.1637T>C
|
ENSP00000512086.1:n.1637T>C
|
|
ENST00000695692.1:n.2060T>C
|
|
|
ENST00000245907.11:c.2696T>C
MANE Select
|
ENSP00000245907.4:p.Val899Ala
|
|
ENST00000245907.10:c.2696T>C
|
ENSP00000245907.4:p.Val899Ala
|
|
ENST00000594005.1:n.272T>C
|
|
|
NM_000064.3:c.2696T>C
|
NP_000055.2:p.Val899Ala
|
|
NM_000064.4:c.2696T>C
MANE Select
|
NP_000055.2:p.Val899Ala
|
|