ENST00000695651.1:n.2008G>A
|
|
|
ENST00000695652.1:c.3537G>A
|
ENSP00000512083.1:p.Trp1179Ter
|
|
ENST00000695653.1:c.1569G>A
|
ENSP00000512084.1:p.Trp523Ter
|
|
ENST00000695654.1:c.2685G>A
|
ENSP00000512085.1:p.Trp895Ter
|
|
ENST00000695655.1:c.2601G>A
|
ENSP00000512086.1:n.2601G>A
|
|
ENST00000695692.1:n.3024G>A
|
|
|
ENST00000245907.11:c.3660G>A
MANE Select
|
ENSP00000245907.4:p.Trp1220Ter
|
|
ENST00000245907.10:c.3660G>A
|
ENSP00000245907.4:p.Trp1220Ter
|
|
ENST00000596238.1:n.103G>A
|
|
|
ENST00000601008.1:c.241+472G>A
|
ENSP00000471384.1:n.241+472G>A
|
|
NM_000064.3:c.3660G>A
|
NP_000055.2:p.Trp1220Ter
|
|
NM_000064.4:c.3660G>A
MANE Select
|
NP_000055.2:p.Trp1220Ter
|
|