ENST00000317357.10:c.1629C>G
MANE Select
|
ENSP00000318900.5:p.Ile543Met
|
|
ENST00000317357.9:c.1629C>G
|
ENSP00000318900.5:p.Ile543Met
|
|
NM_018013.3:c.1629C>G
|
NP_060483.3:p.Ile543Met
|
|
XM_005267041.3:c.1782C>G
|
XP_005267098.1:p.Ile594Met
|
|
XM_005267042.3:c.1686C>G
|
XP_005267099.1:p.Ile562Met
|
|
XM_011535920.1:c.1782C>G
|
XP_011534222.1:p.Ile594Met
|
|
XM_011535921.1:c.1668C>G
|
XP_011534223.1:p.Ile556Met
|
|
XM_011535922.1:c.1041C>G
|
XP_011534224.1:p.Ile347Met
|
|
XM_011535923.1:c.852C>G
|
XP_011534225.1:p.Ile284Met
|
|
XM_005267041.4:c.1782C>G
|
XP_005267098.1:p.Ile594Met
|
|
XM_005267042.4:c.1686C>G
|
XP_005267099.1:p.Ile562Met
|
|
XM_011535920.2:c.1782C>G
|
XP_011534222.1:p.Ile594Met
|
|
XM_011535921.2:c.1668C>G
|
XP_011534223.1:p.Ile556Met
|
|
XM_011535923.2:c.852C>G
|
XP_011534225.1:p.Ile284Met
|
|
XM_017010991.1:c.1182C>G
|
XP_016866480.1:p.Ile394Met
|
|
XM_017010992.1:c.1182C>G
|
XP_016866481.1:p.Ile394Met
|
|
XM_017010993.1:c.1182C>G
|
XP_016866482.1:p.Ile394Met
|
|
XM_017010994.1:c.1182C>G
|
XP_016866483.1:p.Ile394Met
|
|
NM_018013.4:c.1629C>G
MANE Select
|
NP_060483.3:p.Ile543Met
|
|