ENST00000555815.7:c.3894G>T
MANE Select
|
ENSP00000450480.2:p.Arg1298Ser
|
|
ENST00000356865.11:c.3894G>T
|
ENSP00000349325.6:p.Arg1298Ser
|
|
ENST00000555450.2:n.1686G>T
|
|
|
ENST00000555815.6:c.3894G>T
|
ENSP00000450480.2:p.Arg1298Ser
|
|
ENST00000673680.1:n.4556G>T
|
|
|
ENST00000673805.1:n.3239G>T
|
|
|
ENST00000674021.1:n.2221G>T
|
|
|
ENST00000356865.10:c.3894G>T
|
ENSP00000349325.6:p.Arg1298Ser
|
|
ENST00000555815.5:c.*2108G>T
|
ENSP00000450480.1:n.*2108G>T
|
|
NM_024490.3:c.3894G>T
|
NP_077816.1:p.Arg1298Ser
|
|
XM_005268261.3:c.3894G>T
|
XP_005268318.1:p.Arg1298Ser
|
|
XM_011521826.1:c.3894G>T
|
XP_011520128.1:p.Arg1298Ser
|
|
XM_011521827.1:c.3894G>T
|
XP_011520129.1:p.Arg1298Ser
|
|
XM_011521828.1:c.3894G>T
|
XP_011520130.1:p.Arg1298Ser
|
|
XM_011521829.1:c.2979G>T
|
XP_011520131.1:p.Arg993Ser
|
|
XM_011521830.1:c.2556G>T
|
XP_011520132.1:p.Arg852Ser
|
|
XM_005268261.4:c.3894G>T
|
XP_005268318.1:p.Arg1298Ser
|
|
XM_011521826.2:c.3894G>T
|
XP_011520128.1:p.Arg1298Ser
|
|
XM_011521828.2:c.3894G>T
|
XP_011520130.1:p.Arg1298Ser
|
|
XM_011521829.2:c.2979G>T
|
XP_011520131.1:p.Arg993Ser
|
|
XM_011521830.2:c.2718G>T
|
XP_011520132.2:p.Arg906Ser
|
|
XM_017022436.1:c.3453G>T
|
XP_016877925.1:p.Arg1151Ser
|
|
XM_017022437.1:c.2979G>T
|
XP_016877926.1:p.Arg993Ser
|
|
NM_024490.4:c.3894G>T
MANE Select
|
NP_077816.1:p.Arg1298Ser
|
|