ENST00000695651.1:n.2041G=
|
|
|
ENST00000695652.1:c.3570G=
|
ENSP00000512083.1:p.Glu1190=
|
|
ENST00000695653.1:c.1602G=
|
ENSP00000512084.1:p.Glu534=
|
|
ENST00000695654.1:c.2718G=
|
ENSP00000512085.1:p.Glu906=
|
|
ENST00000695655.1:c.2634G=
|
ENSP00000512086.1:n.2634G=
|
|
ENST00000695692.1:n.3057G=
|
|
|
ENST00000245907.11:c.3693G=
MANE Select
|
ENSP00000245907.4:p.Glu1231=
|
|
ENST00000245907.10:c.3693G=
|
ENSP00000245907.4:p.Glu1231=
|
|
ENST00000596238.1:n.136G=
|
|
|
ENST00000601008.1:c.241+505G=
|
ENSP00000471384.1:n.241+505G=
|
|
NM_000064.3:c.3693G=
|
NP_000055.2:p.Glu1231=
|
|
NM_000064.4:c.3693G=
MANE Select
|
NP_000055.2:p.Glu1231=
|
|