ENST00000303115.8:c.1066A=
MANE Select
|
ENSP00000306157.3:p.Ile356=
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|
ENST00000303115.7:c.1066A=
|
ENSP00000306157.3:p.Ile356=
|
|
ENST00000505093.1:c.381A=
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ENSP00000426069.1:n.381A=
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|
ENST00000505875.1:n.364A=
|
|
|
ENST00000514217.5:c.*260A=
|
ENSP00000427688.1:n.*260A=
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|
NM_002185.3:c.1066A=
|
NP_002176.2:p.Ile356=
|
|
NR_120485.1:n.906A=
|
|
|
NM_002185.4:c.1066A=
|
NP_002176.2:p.Ile356=
|
|
NR_120485.2:n.932A=
|
|
|
XM_005248299.4:c.*183A=
|
XP_005248356.1:n.*183A=
|
|
NM_002185.5:c.1066A=
MANE Select
|
NP_002176.2:p.Ile356=
|
|
NR_120485.3:n.890A=
|
|
|