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ENST00000396819.8:c.3475A=
MANE Select
|
ENSP00000380031.5:p.Thr1159=
|
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ENST00000204005.13:c.3565A=
|
ENSP00000204005.10:p.Thr1189=
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ENST00000243562.13:c.1674A=
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ENST00000308370.11:c.3676A=
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ENSP00000311905.8:p.Thr1226=
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ENST00000318809.11:n.484-946A=
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ENST00000396819.7:c.3475A=
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ENSP00000380031.4:p.Thr1159=
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ENST00000593463.5:c.535-946A=
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ENST00000594116.1:n.271A=
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ENST00000595118.5:n.980A=
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ENST00000595665.1:n.535-946A=
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ENST00000597816.5:n.453-946A=
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ENST00000599724.5:c.485-946A=
|
ENSP00000469785.1:n.485-946A=
|
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ENST00000601032.5:c.1112A=
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ENST00000622107.4:n.545-946A=
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ENST00000622457.1:c.385-946A=
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ENST00000622565.4:n.727-946A=
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NM_001042544.1:c.3676A=
|
NP_001036009.1:p.Thr1226=
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NM_001042545.1:c.3475A=
|
NP_001036010.1:p.Thr1159=
|
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NM_003573.2:c.3565A=
|
NP_003564.2:p.Thr1189=
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XM_011527376.1:c.3790A=
|
XP_011525678.1:p.Thr1264=
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XM_011527377.1:c.3709A=
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XP_011525679.1:p.Thr1237=
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XM_011527378.1:c.3709A=
|
XP_011525680.1:p.Thr1237=
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XM_011527379.1:c.3589A=
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XP_011525681.1:p.Thr1197=
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XM_011527380.1:c.3583A=
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XP_011525682.1:p.Thr1195=
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XM_011527381.1:c.3583A=
|
XP_011525683.1:p.Thr1195=
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XM_011527382.1:c.3466A=
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XP_011525684.1:p.Thr1156=
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XM_011527383.1:c.3452-946A=
|
XP_011525685.1:n.3452-946A=
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XM_011527384.1:c.3326-946A=
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XP_011525686.1:n.3326-946A=
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XM_011527385.1:c.3320-946A=
|
XP_011525687.1:n.3320-946A=
|
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XM_011527386.1:c.3194-946A=
|
XP_011525688.1:n.3194-946A=
|
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XM_011527387.1:c.3067A=
|
XP_011525689.1:p.Thr1023=
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XM_011527376.2:c.3790A=
|
XP_011525678.1:p.Thr1264=
|
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XM_011527377.2:c.3709A=
|
XP_011525679.1:p.Thr1237=
|
|
|
XM_011527378.2:c.3709A=
|
XP_011525680.1:p.Thr1237=
|
|
|
XM_011527380.2:c.3583A=
|
XP_011525682.1:p.Thr1195=
|
|
|
XM_011527381.2:c.3583A=
|
XP_011525683.1:p.Thr1195=
|
|
|
XM_011527382.2:c.3466A=
|
XP_011525684.1:p.Thr1156=
|
|
|
XM_011527383.2:c.3452-946A=
|
XP_011525685.1:n.3452-946A=
|
|
|
XM_011527384.2:c.3326-946A=
|
XP_011525686.1:n.3326-946A=
|
|
|
XM_011527385.2:c.3320-946A=
|
XP_011525687.1:n.3320-946A=
|
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|
XM_011527386.2:c.3194-946A=
|
XP_011525688.1:n.3194-946A=
|
|
|
XM_017027352.1:c.3577A=
|
XP_016882841.1:p.Thr1193=
|
|
|
XM_017027353.1:c.3451A=
|
XP_016882842.1:p.Thr1151=
|
|
|
XM_017027354.1:c.3200-946A=
|
XP_016882843.1:n.3200-946A=
|
|
|
NM_001042545.2:c.3475A=
MANE Select
|
NP_001036010.1:p.Thr1159=
|
|
