ENST00000695651.1:n.1073G>T
|
|
|
ENST00000695652.1:c.2602G>T
|
ENSP00000512083.1:p.Glu868Ter
|
|
ENST00000695653.1:c.634G>T
|
ENSP00000512084.1:p.Glu212Ter
|
|
ENST00000695654.1:c.1849G>T
|
ENSP00000512085.1:p.Glu617Ter
|
|
ENST00000695655.1:c.1666G>T
|
ENSP00000512086.1:n.1666G>T
|
|
ENST00000695692.1:n.2089G>T
|
|
|
ENST00000245907.11:c.2725G>T
MANE Select
|
ENSP00000245907.4:p.Glu909Ter
|
|
ENST00000245907.10:c.2725G>T
|
ENSP00000245907.4:p.Glu909Ter
|
|
ENST00000594005.1:n.301G>T
|
|
|
NM_000064.3:c.2725G>T
|
NP_000055.2:p.Glu909Ter
|
|
NM_000064.4:c.2725G>T
MANE Select
|
NP_000055.2:p.Glu909Ter
|
|