ENST00000392017.9:c.853A>T
MANE Select
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ENSP00000375872.4:p.Arg285Ter
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ENST00000347464.9:c.364A>T
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ENSP00000318259.6:p.Arg122Ter
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|
ENST00000373525.9:c.421A>T
|
ENSP00000362625.5:p.Arg141Ter
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ENST00000392017.8:c.853A>T
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ENSP00000375872.4:p.Arg285Ter
|
|
ENST00000392018.1:c.904A>T
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ENSP00000375873.1:p.Arg302Ter
|
|
ENST00000392020.8:c.796A>T
|
ENSP00000375875.4:p.Arg266Ter
|
|
ENST00000392021.7:c.*734A>T
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ENSP00000375876.3:n.*734A>T
|
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ENST00000419681.5:c.364A>T
|
ENSP00000398773.1:p.Arg122Ter
|
|
ENST00000444735.5:c.472A>T
|
ENSP00000409215.1:p.Arg158Ter
|
|
ENST00000474148.5:n.1648A>T
|
|
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ENST00000479942.5:n.999A>T
|
|
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ENST00000492298.5:n.374A>T
|
|
|
ENST00000498620.5:n.360A>T
|
|
|
NM_001190266.1:c.601A>T
|
NP_001177195.1:p.Arg201Ter
|
|
NM_001190267.1:c.505A>T
|
NP_001177196.1:p.Arg169Ter
|
|
NM_017974.3:c.796A>T
|
NP_060444.3:p.Arg266Ter
|
|
NM_030803.6:c.853A>T
|
NP_110430.5:p.Arg285Ter
|
|
NM_198890.2:c.364A>T
|
NP_942593.2:p.Arg122Ter
|
|
XM_005246082.1:c.904A>T
|
XP_005246139.1:p.Arg302Ter
|
|
XM_005246084.1:c.472A>T
|
XP_005246141.1:p.Arg158Ter
|
|
XM_005246086.1:c.421A>T
|
XP_005246143.1:p.Arg141Ter
|
|
XM_006712608.1:c.652A>T
|
XP_006712671.1:p.Arg218Ter
|
|
XR_241242.1:n.1098A>T
|
|
|
NM_001363742.1:c.904A>T
|
NP_001350671.1:p.Arg302Ter
|
|
XM_005246084.2:c.472A>T
|
XP_005246141.1:p.Arg158Ter
|
|
XM_005246086.2:c.421A>T
|
XP_005246143.1:p.Arg141Ter
|
|
XM_006712608.3:c.652A>T
|
XP_006712671.1:p.Arg218Ter
|
|
XR_001738801.2:n.1034A>T
|
|
|
XR_241242.3:n.1085A>T
|
|
|
NM_030803.7:c.853A>T
MANE Select
|
NP_110430.5:p.Arg285Ter
|
|
NM_001190266.2:c.601A>T
|
NP_001177195.1:p.Arg201Ter
|
|
NM_001190267.2:c.505A>T
|
NP_001177196.1:p.Arg169Ter
|
|
NM_001363742.2:c.904A>T
|
NP_001350671.1:p.Arg302Ter
|
|
NM_017974.4:c.796A>T
|
NP_060444.3:p.Arg266Ter
|
|
NM_198890.3:c.364A>T
|
NP_942593.2:p.Arg122Ter
|
|