ENST00000695651.1:n.2977T>A
|
|
|
ENST00000695653.1:c.2538T>A
|
ENSP00000512084.1:p.Tyr846Ter
|
|
ENST00000695654.1:c.3654T>A
|
ENSP00000512085.1:p.Tyr1218Ter
|
|
ENST00000695689.1:c.600T>A
|
ENSP00000512101.1:n.600T>A
|
|
ENST00000695690.1:n.1694T>A
|
|
|
ENST00000695691.1:n.1490T>A
|
|
|
ENST00000245907.11:c.4629T>A
MANE Select
|
ENSP00000245907.4:p.Tyr1543Ter
|
|
ENST00000245907.10:c.4629T>A
|
ENSP00000245907.4:p.Tyr1543Ter
|
|
ENST00000599668.1:n.249T>A
|
|
|
ENST00000599899.5:n.1588T>A
|
|
|
ENST00000601008.1:c.242-1168T>A
|
ENSP00000471384.1:n.242-1168T>A
|
|
ENST00000602229.1:c.76T>A
|
|
|
NM_000064.3:c.4629T>A
|
NP_000055.2:p.Tyr1543Ter
|
|
NM_000064.4:c.4629T>A
MANE Select
|
NP_000055.2:p.Tyr1543Ter
|
|