ENST00000284885.8:c.2630T>G
MANE Select
|
ENSP00000284885.3:p.Ile877Ser
|
|
ENST00000284885.7:c.2630T>G
|
ENSP00000284885.3:p.Ile877Ser
|
|
NM_002772.2:c.2630T>G
|
NP_002763.2:p.Ile877Ser
|
|
XM_011529654.1:c.2765T>G
|
XP_011527956.1:p.Ile922Ser
|
|
XM_011529655.1:c.2765T>G
|
XP_011527957.1:p.Ile922Ser
|
|
XM_011529656.1:c.2765T>G
|
XP_011527958.1:p.Ile922Ser
|
|
XM_011529657.1:c.2720T>G
|
XP_011527959.1:p.Ile907Ser
|
|
XM_011529658.1:c.2684T>G
|
XP_011527960.1:p.Ile895Ser
|
|
XM_011529659.1:c.2675T>G
|
XP_011527961.1:p.Ile892Ser
|
|
XM_011529654.2:c.2765T>G
|
XP_011527956.1:p.Ile922Ser
|
|
XM_011529656.2:c.2765T>G
|
XP_011527958.1:p.Ile922Ser
|
|
XM_011529657.2:c.2720T>G
|
XP_011527959.1:p.Ile907Ser
|
|
XM_011529658.2:c.2684T>G
|
XP_011527960.1:p.Ile895Ser
|
|
NM_002772.3:c.2630T>G
MANE Select
|
NP_002763.3:p.Ile877Ser
|
|