ENST00000695651.1:n.2524C>A
|
|
|
ENST00000695653.1:c.2085C>A
|
ENSP00000512084.1:p.Tyr695Ter
|
|
ENST00000695654.1:c.3201C>A
|
ENSP00000512085.1:p.Tyr1067Ter
|
|
ENST00000695689.1:c.147C>A
|
ENSP00000512101.1:n.147C>A
|
|
ENST00000695690.1:n.367C>A
|
|
|
ENST00000695691.1:n.367C>A
|
|
|
ENST00000245907.11:c.4176C>A
MANE Select
|
ENSP00000245907.4:p.Tyr1392Ter
|
|
ENST00000245907.10:c.4176C>A
|
ENSP00000245907.4:p.Tyr1392Ter
|
|
ENST00000596548.1:c.297C>A
|
ENSP00000469744.1:p.Tyr99Ter
|
|
ENST00000599899.5:n.1135C>A
|
|
|
ENST00000601008.1:c.242-4268C>A
|
ENSP00000471384.1:n.242-4268C>A
|
|
NM_000064.3:c.4176C>A
|
NP_000055.2:p.Tyr1392Ter
|
|
NM_000064.4:c.4176C>A
MANE Select
|
NP_000055.2:p.Tyr1392Ter
|
|