|
ENST00000278407.9:c.1372G>A
MANE Select
|
ENSP00000278407.4:p.Ala458Thr
|
|
|
ENST00000528996.2:c.*269G>A
|
ENSP00000431226.2:n.*269G>A
|
|
|
ENST00000531605.2:c.*1148G>A
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ENSP00000503752.1:n.*1148G>A
|
|
|
ENST00000619430.2:c.1168G>A
|
ENSP00000478572.2:p.Ala390Thr
|
|
|
ENST00000676670.1:c.1372G>A
|
ENSP00000504807.1:p.Ala458Thr
|
|
|
ENST00000676741.1:n.2454G>A
|
|
|
|
ENST00000677624.1:c.*792G>A
|
ENSP00000503979.1:n.*792G>A
|
|
|
ENST00000677625.1:c.1318G>A
|
ENSP00000502857.1:p.Ala440Thr
|
|
|
ENST00000677856.1:n.1625G>A
|
|
|
|
ENST00000677915.1:c.*269G>A
|
ENSP00000503118.1:n.*269G>A
|
|
|
ENST00000678533.1:c.*926G>A
|
ENSP00000503873.1:n.*926G>A
|
|
|
ENST00000678592.1:c.*312G>A
|
ENSP00000504424.1:n.*312G>A
|
|
|
ENST00000278407.8:c.1372G>A
|
ENSP00000278407.4:p.Ala458Thr
|
|
|
ENST00000340687.10:c.1261G>A
|
ENSP00000341861.6:p.Ala421Thr
|
|
|
ENST00000378323.8:c.1387G>A
|
ENSP00000367574.4:p.Ala463Thr
|
|
|
ENST00000378324.6:c.1216G>A
|
ENSP00000367575.2:p.Ala406Thr
|
|
|
ENST00000403558.1:c.1501G>A
|
ENSP00000384420.1:p.Ala501Thr
|
|
|
ENST00000528996.1:c.573G>A
|
ENSP00000431226.1:n.573G>A
|
|
|
ENST00000530113.1:n.829G>A
|
|
|
|
ENST00000531133.5:c.873G>A
|
ENSP00000435431.1:n.873G>A
|
|
|
ENST00000531797.5:c.*397G>A
|
ENSP00000432554.1:n.*397G>A
|
|
|
ENST00000619430.1:c.503G>A
|
ENSP00000478572.1:n.503G>A
|
|
|
NM_000062.2:c.1372G>A , LRG_105t1:c.1372G>A
|
NP_000053.2:p.Ala458Thr
|
|
|
NM_001032295.1:c.1372G>A
|
NP_001027466.1:p.Ala458Thr
|
|
|
NM_000062.3:c.1372G>A
MANE Select
|
NP_000053.2:p.Ala458Thr
|
|
|
NM_001032295.2:c.1372G>A
|
NP_001027466.1:p.Ala458Thr
|
|
