ENST00000383788.10:c.671C>T
MANE Select
|
ENSP00000373298.3:p.Ala224Val
|
|
ENST00000604401.2:n.667C>T
|
|
|
ENST00000679838.1:c.*433C>T
|
ENSP00000505708.1:n.*433C>T
|
|
ENST00000680545.1:n.437C>T
|
|
|
ENST00000681097.1:c.671C>T
|
ENSP00000505397.1:p.Ala224Val
|
|
ENST00000383781.8:c.641C>T
|
ENSP00000373291.3:p.Ala214Val
|
|
ENST00000383786.9:c.569C>T
|
ENSP00000373296.3:p.Ala190Val
|
|
ENST00000383788.9:c.671C>T
|
ENSP00000373298.3:p.Ala224Val
|
|
ENST00000603808.5:c.671C>T
|
ENSP00000474271.1:p.Ala224Val
|
|
ENST00000605797.1:c.500C>T
|
ENSP00000474936.1:p.Ala167Val
|
|
NM_005677.3:c.671C>T
|
NP_005668.2:p.Ala224Val
|
|
NM_080538.2:c.641C>T
|
NP_536799.1:p.Ala214Val
|
|
NM_080539.3:c.569C>T
|
NP_536800.2:p.Ala190Val
|
|
NM_005677.4:c.671C>T
MANE Select
|
NP_005668.2:p.Ala224Val
|
|
NM_080539.4:c.569C>T
|
NP_536800.2:p.Ala190Val
|
|