ENST00000403665.7:c.1444G>T
MANE Select
|
ENSP00000384957.2:p.Ala482Ser
|
|
ENST00000264691.4:c.140G>T
|
|
|
ENST00000264692.8:c.1282G>T
|
ENSP00000264692.5:p.Ala428Ser
|
|
ENST00000403665.6:c.1444G>T
|
ENSP00000384957.2:p.Ala482Ser
|
|
NM_000128.3:c.1444G>T , LRG_583t1:c.1444G>T
|
NP_000119.1:p.Ala482Ser
|
|
XM_005262821.2:c.1447G>T
|
XP_005262878.1:p.Ala483Ser
|
|
XM_005262822.2:c.1447G>T
|
XP_005262879.1:p.Ala483Ser
|
|
XM_005262823.2:c.1177G>T
|
XP_005262880.1:p.Ala393Ser
|
|
XM_005262824.1:c.1447G>T
|
XP_005262881.1:p.Ala483Ser
|
|
XM_006714137.1:c.1399G>T
|
XP_006714200.1:p.Ala467Ser
|
|
XR_938706.1:n.1852G>T
|
|
|
XR_938707.1:n.1852G>T
|
|
|
XM_005262821.4:c.1447G>T
|
XP_005262878.1:p.Ala483Ser
|
|
XM_005262822.4:c.1447G>T
|
XP_005262879.1:p.Ala483Ser
|
|
XM_005262823.4:c.1177G>T
|
XP_005262880.1:p.Ala393Ser
|
|
XM_006714137.3:c.1399G>T
|
XP_006714200.1:p.Ala467Ser
|
|
XR_001741172.2:n.1918G>T
|
|
|
NM_000128.4:c.1444G>T
MANE Select
|
NP_000119.1:p.Ala482Ser
|
|