ENST00000695651.1:n.2051T>C
|
|
|
ENST00000695652.1:c.3580T>C
|
ENSP00000512083.1:p.Tyr1194His
|
|
ENST00000695653.1:c.1612T>C
|
ENSP00000512084.1:p.Tyr538His
|
|
ENST00000695654.1:c.2728T>C
|
ENSP00000512085.1:p.Tyr910His
|
|
ENST00000695655.1:c.2644T>C
|
ENSP00000512086.1:n.2644T>C
|
|
ENST00000695692.1:n.3067T>C
|
|
|
ENST00000245907.11:c.3703T>C
MANE Select
|
ENSP00000245907.4:p.Tyr1235His
|
|
ENST00000245907.10:c.3703T>C
|
ENSP00000245907.4:p.Tyr1235His
|
|
ENST00000596238.1:n.146T>C
|
|
|
ENST00000601008.1:c.241+515T>C
|
ENSP00000471384.1:n.241+515T>C
|
|
NM_000064.3:c.3703T>C
|
NP_000055.2:p.Tyr1235His
|
|
NM_000064.4:c.3703T>C
MANE Select
|
NP_000055.2:p.Tyr1235His
|
|