ENST00000355808.10:c.643T>C
|
ENSP00000348062.6:p.Tyr215His
|
|
ENST00000379805.4:c.*314T>C
|
ENSP00000369133.3:n.*314T>C
|
|
ENST00000417819.6:c.706T>C
|
ENSP00000404616.2:p.Tyr236His
|
|
ENST00000423505.6:c.736T>C
|
ENSP00000406473.2:p.Tyr246His
|
|
ENST00000481733.2:n.417T>C
|
|
|
ENST00000696704.1:c.437T>C
|
ENSP00000512823.1:p.Leu146Ser
|
|
ENST00000696705.1:c.*77T>C
|
ENSP00000512824.1:n.*77T>C
|
|
ENST00000422285.7:c.622T>C
MANE Select
|
ENSP00000394382.2:p.Tyr208His
|
|
ENST00000379806.9:c.736T>C
|
ENSP00000369134.5:p.Tyr246His
|
|
ENST00000422285.6:c.622T>C
|
ENSP00000394382.2:p.Tyr208His
|
|
ENST00000479146.1:n.457T>C
|
|
|
ENST00000481733.1:n.50T>C
|
|
|
ENST00000540249.5:c.529T>C
|
ENSP00000440761.1:p.Tyr177His
|
|
ENST00000545074.5:c.643T>C
|
ENSP00000438550.1:p.Tyr215His
|
|
NM_000284.3:c.622T>C
|
NP_000275.1:p.Tyr208His
|
|
NM_001173454.1:c.736T>C
|
NP_001166925.1:p.Tyr246His
|
|
NM_001173455.1:c.643T>C
|
NP_001166926.1:p.Tyr215His
|
|
NM_001173456.1:c.529T>C
|
NP_001166927.1:p.Tyr177His
|
|
XM_011545531.1:c.757T>C
|
XP_011543833.1:p.Tyr253His
|
|
XM_011545532.1:c.664T>C
|
XP_011543834.1:p.Tyr222His
|
|
XM_017029574.2:c.643T>C
|
XP_016885063.1:p.Tyr215His
|
|
NM_000284.4:c.622T>C
MANE Select
|
NP_000275.1:p.Tyr208His
|
|
NM_001173454.2:c.736T>C
|
NP_001166925.1:p.Tyr246His
|
|
NM_001173455.2:c.643T>C
|
NP_001166926.1:p.Tyr215His
|
|
NM_001173456.2:c.529T>C
|
NP_001166927.1:p.Tyr177His
|
|