ENST00000383788.10:c.794C>A
MANE Select
|
ENSP00000373298.3:p.Pro265His
|
|
ENST00000604401.2:n.790C>A
|
|
|
ENST00000679838.1:c.*556C>A
|
ENSP00000505708.1:n.*556C>A
|
|
ENST00000680545.1:n.560C>A
|
|
|
ENST00000681097.1:c.794C>A
|
ENSP00000505397.1:p.Pro265His
|
|
ENST00000383781.8:c.764C>A
|
ENSP00000373291.3:p.Pro255His
|
|
ENST00000383786.9:c.692C>A
|
ENSP00000373296.3:p.Pro231His
|
|
ENST00000383788.9:c.794C>A
|
ENSP00000373298.3:p.Pro265His
|
|
ENST00000603808.5:c.794C>A
|
ENSP00000474271.1:p.Pro265His
|
|
NM_005677.3:c.794C>A
|
NP_005668.2:p.Pro265His
|
|
NM_080538.2:c.764C>A
|
NP_536799.1:p.Pro255His
|
|
NM_080539.3:c.692C>A
|
NP_536800.2:p.Pro231His
|
|
NM_005677.4:c.794C>A
MANE Select
|
NP_005668.2:p.Pro265His
|
|
NM_080539.4:c.692C>A
|
NP_536800.2:p.Pro231His
|
|