ENST00000307179.9:c.2057C>A
MANE Select
|
ENSP00000302239.4:p.Ser686Ter
|
|
ENST00000307179.8:c.2057C>A
|
ENSP00000302239.4:p.Ser686Ter
|
|
ENST00000396444.7:c.2057C>A
|
ENSP00000379721.3:p.Ser686Ter
|
|
ENST00000425032.7:c.1739C>A
|
ENSP00000412682.3:p.Ser580Ter
|
|
ENST00000561206.1:n.474C>A
|
|
|
NM_001128610.2:c.2057C>A
|
NP_001122082.1:p.Ser686Ter
|
|
NM_001283049.1:c.1739C>A
|
NP_001269978.1:p.Ser580Ter
|
|
NM_005154.4:c.2057C>A
|
NP_005145.3:p.Ser686Ter
|
|
XM_006720761.2:c.2057C>A
|
XP_006720824.1:p.Ser686Ter
|
|
XM_006720762.2:c.1970C>A
|
XP_006720825.1:p.Ser657Ter
|
|
XM_011522193.1:c.2057C>A
|
XP_011520495.1:p.Ser686Ter
|
|
XM_011522194.1:c.1385C>A
|
XP_011520496.1:p.Ser462Ter
|
|
XM_006720761.3:c.2057C>A
|
XP_006720824.1:p.Ser686Ter
|
|
XM_006720762.3:c.1970C>A
|
XP_006720825.1:p.Ser657Ter
|
|
XM_011522193.3:c.2057C>A
|
XP_011520495.1:p.Ser686Ter
|
|
XM_017022718.1:c.1970C>A
|
XP_016878207.1:p.Ser657Ter
|
|
XM_017022719.2:c.1970C>A
|
XP_016878208.1:p.Ser657Ter
|
|
XM_017022720.2:c.1970C>A
|
XP_016878209.1:p.Ser657Ter
|
|
XM_017022721.2:c.1487C>A
|
XP_016878210.1:p.Ser496Ter
|
|
XM_017022722.1:c.1487C>A
|
XP_016878211.1:p.Ser496Ter
|
|
XM_024450098.1:c.1487C>A
|
XP_024305866.1:p.Ser496Ter
|
|
NM_005154.5:c.2057C>A
MANE Select
|
NP_005145.3:p.Ser686Ter
|
|
NM_001128610.3:c.2057C>A
|
NP_001122082.1:p.Ser686Ter
|
|
NM_001283049.2:c.1739C>A
|
NP_001269978.1:p.Ser580Ter
|
|