ENST00000436784.7:c.*3G=
MANE Select
|
ENSP00000389175.2:n.*3G=
|
|
ENST00000436784.6:c.*3G=
|
ENSP00000389175.2:n.*3G=
|
|
ENST00000461183.5:c.847G=
|
ENSP00000417264.1:p.Ala283=
|
|
ENST00000471180.5:c.718G=
|
ENSP00000417526.1:p.Ala240=
|
|
ENST00000473032.5:c.613G=
|
ENSP00000418951.1:p.Ala205=
|
|
ENST00000486393.5:c.*938G=
|
ENSP00000419868.1:n.*938G=
|
|
ENST00000489173.1:n.1869G=
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|
|
NM_145262.3:c.*3G=
|
NP_660305.2:n.*3G=
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|
NR_026699.1:n.1673G=
|
|
|
NR_026700.1:n.779G=
|
|
|
NR_026701.1:n.1671G=
|
|
|
NR_026702.1:n.709G=
|
|
|
XM_005264878.2:c.*694G=
|
XP_005264935.1:n.*694G=
|
|
XR_245095.2:n.2826G=
|
|
|
XM_017005730.1:c.*3G=
|
XP_016861219.1:n.*3G=
|
|
XM_024453351.1:c.*3G=
|
XP_024309119.1:n.*3G=
|
|
XM_024453352.1:c.*694G=
|
XP_024309120.1:n.*694G=
|
|
XR_001740022.2:n.3477G=
|
|
|
XR_001740023.2:n.3001G=
|
|
|
XR_245095.4:n.2827G=
|
|
|
NM_145262.4:c.*3G=
MANE Select
|
NP_660305.2:n.*3G=
|
|
NR_026699.2:n.1665G=
|
|
|
NR_026700.2:n.771G=
|
|
|
NR_026701.2:n.1663G=
|
|
|
NR_026702.2:n.701G=
|
|
|
NM_001144951.2:c.*694G=
|
NP_001138423.1:n.*694G=
|
|