ENST00000695651.1:n.2287G>A
|
|
|
ENST00000695653.1:c.1848G>A
|
ENSP00000512084.1:p.Trp616Ter
|
|
ENST00000695654.1:c.2964G>A
|
ENSP00000512085.1:p.Trp988Ter
|
|
ENST00000695690.1:n.130G>A
|
|
|
ENST00000695691.1:n.130G>A
|
|
|
ENST00000245907.11:c.3939G>A
MANE Select
|
ENSP00000245907.4:p.Trp1313Ter
|
|
ENST00000245907.10:c.3939G>A
|
ENSP00000245907.4:p.Trp1313Ter
|
|
ENST00000596238.1:n.382G>A
|
|
|
ENST00000596548.1:c.21G>A
|
ENSP00000469744.1:p.Trp7Ter
|
|
ENST00000601008.1:c.241+1728G>A
|
ENSP00000471384.1:n.241+1728G>A
|
|
NM_000064.3:c.3939G>A
|
NP_000055.2:p.Trp1313Ter
|
|
NM_000064.4:c.3939G>A
MANE Select
|
NP_000055.2:p.Trp1313Ter
|
|