ENST00000403665.7:c.1322T>G
MANE Select
|
ENSP00000384957.2:p.Ile441Ser
|
|
ENST00000264691.4:c.18T>G
|
|
|
ENST00000264692.8:c.1160T>G
|
ENSP00000264692.5:p.Ile387Ser
|
|
ENST00000403665.6:c.1322T>G
|
ENSP00000384957.2:p.Ile441Ser
|
|
NM_000128.3:c.1322T>G , LRG_583t1:c.1322T>G
|
NP_000119.1:p.Ile441Ser
|
|
XM_005262821.2:c.1325T>G
|
XP_005262878.1:p.Ile442Ser
|
|
XM_005262822.2:c.1325T>G
|
XP_005262879.1:p.Ile442Ser
|
|
XM_005262823.2:c.1055T>G
|
XP_005262880.1:p.Ile352Ser
|
|
XM_005262824.1:c.1325T>G
|
XP_005262881.1:p.Ile442Ser
|
|
XM_006714137.1:c.1277T>G
|
XP_006714200.1:p.Ile426Ser
|
|
XR_938706.1:n.1730T>G
|
|
|
XR_938707.1:n.1730T>G
|
|
|
XM_005262821.4:c.1325T>G
|
XP_005262878.1:p.Ile442Ser
|
|
XM_005262822.4:c.1325T>G
|
XP_005262879.1:p.Ile442Ser
|
|
XM_005262823.4:c.1055T>G
|
XP_005262880.1:p.Ile352Ser
|
|
XM_006714137.3:c.1277T>G
|
XP_006714200.1:p.Ile426Ser
|
|
XR_001741172.2:n.1796T>G
|
|
|
NM_000128.4:c.1322T>G
MANE Select
|
NP_000119.1:p.Ile441Ser
|
|