ENST00000695651.1:n.2312G>A
|
|
|
ENST00000695653.1:c.1873G>A
|
ENSP00000512084.1:p.Glu625Lys
|
|
ENST00000695654.1:c.2989G>A
|
ENSP00000512085.1:p.Glu997Lys
|
|
ENST00000695690.1:n.155G>A
|
|
|
ENST00000695691.1:n.155G>A
|
|
|
ENST00000245907.11:c.3964G>A
MANE Select
|
ENSP00000245907.4:p.Glu1322Lys
|
|
ENST00000245907.10:c.3964G>A
|
ENSP00000245907.4:p.Glu1322Lys
|
|
ENST00000596238.1:n.407G>A
|
|
|
ENST00000596548.1:c.46G>A
|
ENSP00000469744.1:p.Glu16Lys
|
|
ENST00000601008.1:c.241+1753G>A
|
ENSP00000471384.1:n.241+1753G>A
|
|
NM_000064.3:c.3964G>A
|
NP_000055.2:p.Glu1322Lys
|
|
NM_000064.4:c.3964G>A
MANE Select
|
NP_000055.2:p.Glu1322Lys
|
|