ENST00000695651.1:n.2831C>A
|
|
|
ENST00000695653.1:c.2392C>A
|
ENSP00000512084.1:p.Pro798Thr
|
|
ENST00000695654.1:c.3508C>A
|
ENSP00000512085.1:p.Pro1170Thr
|
|
ENST00000695689.1:c.454C>A
|
ENSP00000512101.1:n.454C>A
|
|
ENST00000695690.1:n.1548C>A
|
|
|
ENST00000695691.1:n.1344C>A
|
|
|
ENST00000245907.11:c.4483C>A
MANE Select
|
ENSP00000245907.4:p.Pro1495Thr
|
|
ENST00000245907.10:c.4483C>A
|
ENSP00000245907.4:p.Pro1495Thr
|
|
ENST00000599668.1:n.78C>A
|
|
|
ENST00000599899.5:n.1442C>A
|
|
|
ENST00000601008.1:c.242-1512C>A
|
ENSP00000471384.1:n.242-1512C>A
|
|
NM_000064.3:c.4483C>A
|
NP_000055.2:p.Pro1495Thr
|
|
NM_000064.4:c.4483C>A
MANE Select
|
NP_000055.2:p.Pro1495Thr
|
|