ENST00000695651.1:n.2630T>C
|
|
|
ENST00000695653.1:c.2191T>C
|
ENSP00000512084.1:p.Tyr731His
|
|
ENST00000695654.1:c.3307T>C
|
ENSP00000512085.1:p.Tyr1103His
|
|
ENST00000695689.1:c.253T>C
|
ENSP00000512101.1:n.253T>C
|
|
ENST00000695690.1:n.473T>C
|
|
|
ENST00000695691.1:n.473T>C
|
|
|
ENST00000245907.11:c.4282T>C
MANE Select
|
ENSP00000245907.4:p.Tyr1428His
|
|
ENST00000245907.10:c.4282T>C
|
ENSP00000245907.4:p.Tyr1428His
|
|
ENST00000596548.1:c.403T>C
|
ENSP00000469744.1:p.Tyr135His
|
|
ENST00000599899.5:n.1241T>C
|
|
|
ENST00000601008.1:c.242-4051T>C
|
ENSP00000471384.1:n.242-4051T>C
|
|
NM_000064.3:c.4282T>C
|
NP_000055.2:p.Tyr1428His
|
|
NM_000064.4:c.4282T>C
MANE Select
|
NP_000055.2:p.Tyr1428His
|
|