ENST00000403665.7:c.1151T>G
MANE Select
|
ENSP00000384957.2:p.Ile384Ser
|
|
ENST00000264692.8:c.989T>G
|
ENSP00000264692.5:p.Ile330Ser
|
|
ENST00000403665.6:c.1151T>G
|
ENSP00000384957.2:p.Ile384Ser
|
|
NM_000128.3:c.1151T>G , LRG_583t1:c.1151T>G
|
NP_000119.1:p.Ile384Ser
|
|
XM_005262821.2:c.1154T>G
|
XP_005262878.1:p.Ile385Ser
|
|
XM_005262822.2:c.1154T>G
|
XP_005262879.1:p.Ile385Ser
|
|
XM_005262823.2:c.884T>G
|
XP_005262880.1:p.Ile295Ser
|
|
XM_005262824.1:c.1154T>G
|
XP_005262881.1:p.Ile385Ser
|
|
XM_006714137.1:c.1106T>G
|
XP_006714200.1:p.Ile369Ser
|
|
XR_938706.1:n.1559T>G
|
|
|
XR_938707.1:n.1559T>G
|
|
|
XM_005262821.4:c.1154T>G
|
XP_005262878.1:p.Ile385Ser
|
|
XM_005262822.4:c.1154T>G
|
XP_005262879.1:p.Ile385Ser
|
|
XM_005262823.4:c.884T>G
|
XP_005262880.1:p.Ile295Ser
|
|
XM_006714137.3:c.1106T>G
|
XP_006714200.1:p.Ile369Ser
|
|
XM_017007884.2:c.*2123T>G
|
XP_016863373.1:n.*2123T>G
|
|
XM_017007885.2:c.*19T>G
|
XP_016863374.1:n.*19T>G
|
|
XR_001741172.2:n.1625T>G
|
|
|
NM_000128.4:c.1151T>G
MANE Select
|
NP_000119.1:p.Ile384Ser
|
|