ENST00000266771.10:c.810C>T
MANE Select
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ENSP00000266771.5:p.Ser270=
|
|
ENST00000266771.9:c.810C>T
|
ENSP00000266771.5:p.Ser270=
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|
ENST00000366292.6:n.1122C>T
|
|
|
ENST00000376740.8:c.389C>T
|
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ENST00000376744.8:c.646C>T
|
|
|
ENST00000539703.1:n.460C>T
|
|
|
ENST00000614634.1:c.-33C>T
|
ENSP00000483143.1:n.-33C>T
|
|
NM_145648.3:c.810C>T
|
NP_663623.1:p.Ser270=
|
|
XM_011537895.1:c.960C>T
|
XP_011536197.1:p.Ser320=
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XR_429081.2:n.833C>T
|
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XR_944494.1:n.983C>T
|
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XR_944495.1:n.983C>T
|
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XR_944496.1:n.983C>T
|
|
|
XR_944497.1:n.983C>T
|
|
|
XM_017018791.1:c.960C>T
|
XP_016874280.1:p.Ser320=
|
|
XM_017018792.1:c.960C>T
|
XP_016874281.1:p.Ser320=
|
|
XM_017018793.1:c.810C>T
|
XP_016874282.1:p.Ser270=
|
|
XR_002957287.1:n.833C>T
|
|
|
XR_944496.2:n.983C>T
|
|
|
NM_145648.4:c.810C>T
MANE Select
|
NP_663623.1:p.Ser270=
|
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