ENST00000396819.8:c.3456C>T
MANE Select
|
ENSP00000380031.5:p.Arg1152=
|
|
ENST00000204005.13:c.3546C>T
|
ENSP00000204005.10:p.Arg1182=
|
|
ENST00000243562.13:c.1655C>T
|
|
|
ENST00000308370.11:c.3657C>T
|
ENSP00000311905.8:p.Arg1219=
|
|
ENST00000318809.11:n.484-965C>T
|
|
|
ENST00000396819.7:c.3456C>T
|
ENSP00000380031.4:p.Arg1152=
|
|
ENST00000593463.5:c.535-965C>T
|
|
|
ENST00000594116.1:n.252C>T
|
|
|
ENST00000595118.5:n.961C>T
|
|
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ENST00000595665.1:n.535-965C>T
|
|
|
ENST00000597816.5:n.453-965C>T
|
|
|
ENST00000599724.5:c.485-965C>T
|
ENSP00000469785.1:n.485-965C>T
|
|
ENST00000601032.5:c.1093C>T
|
|
|
ENST00000622107.4:n.545-965C>T
|
|
|
ENST00000622457.1:c.385-965C>T
|
|
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ENST00000622565.4:n.727-965C>T
|
|
|
NM_001042544.1:c.3657C>T
|
NP_001036009.1:p.Arg1219=
|
|
NM_001042545.1:c.3456C>T
|
NP_001036010.1:p.Arg1152=
|
|
NM_003573.2:c.3546C>T
|
NP_003564.2:p.Arg1182=
|
|
XM_011527376.1:c.3771C>T
|
XP_011525678.1:p.Arg1257=
|
|
XM_011527377.1:c.3690C>T
|
XP_011525679.1:p.Arg1230=
|
|
XM_011527378.1:c.3690C>T
|
XP_011525680.1:p.Arg1230=
|
|
XM_011527379.1:c.3570C>T
|
XP_011525681.1:p.Arg1190=
|
|
XM_011527380.1:c.3564C>T
|
XP_011525682.1:p.Arg1188=
|
|
XM_011527381.1:c.3564C>T
|
XP_011525683.1:p.Arg1188=
|
|
XM_011527382.1:c.3447C>T
|
XP_011525684.1:p.Arg1149=
|
|
XM_011527383.1:c.3452-965C>T
|
XP_011525685.1:n.3452-965C>T
|
|
XM_011527384.1:c.3326-965C>T
|
XP_011525686.1:n.3326-965C>T
|
|
XM_011527385.1:c.3320-965C>T
|
XP_011525687.1:n.3320-965C>T
|
|
XM_011527386.1:c.3194-965C>T
|
XP_011525688.1:n.3194-965C>T
|
|
XM_011527387.1:c.3048C>T
|
XP_011525689.1:p.Arg1016=
|
|
XM_011527376.2:c.3771C>T
|
XP_011525678.1:p.Arg1257=
|
|
XM_011527377.2:c.3690C>T
|
XP_011525679.1:p.Arg1230=
|
|
XM_011527378.2:c.3690C>T
|
XP_011525680.1:p.Arg1230=
|
|
XM_011527380.2:c.3564C>T
|
XP_011525682.1:p.Arg1188=
|
|
XM_011527381.2:c.3564C>T
|
XP_011525683.1:p.Arg1188=
|
|
XM_011527382.2:c.3447C>T
|
XP_011525684.1:p.Arg1149=
|
|
XM_011527383.2:c.3452-965C>T
|
XP_011525685.1:n.3452-965C>T
|
|
XM_011527384.2:c.3326-965C>T
|
XP_011525686.1:n.3326-965C>T
|
|
XM_011527385.2:c.3320-965C>T
|
XP_011525687.1:n.3320-965C>T
|
|
XM_011527386.2:c.3194-965C>T
|
XP_011525688.1:n.3194-965C>T
|
|
XM_017027352.1:c.3558C>T
|
XP_016882841.1:p.Arg1186=
|
|
XM_017027353.1:c.3432C>T
|
XP_016882842.1:p.Arg1144=
|
|
XM_017027354.1:c.3200-965C>T
|
XP_016882843.1:n.3200-965C>T
|
|
NM_001042545.2:c.3456C>T
MANE Select
|
NP_001036010.1:p.Arg1152=
|
|