ENST00000278407.9:c.1412T>C
MANE Select
|
ENSP00000278407.4:p.Phe471Ser
|
|
ENST00000528996.2:c.*309T>C
|
ENSP00000431226.2:n.*309T>C
|
|
ENST00000531605.2:c.*1188T>C
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ENSP00000503752.1:n.*1188T>C
|
|
ENST00000619430.2:c.1208T>C
|
ENSP00000478572.2:p.Phe403Ser
|
|
ENST00000676670.1:c.1412T>C
|
ENSP00000504807.1:p.Phe471Ser
|
|
ENST00000676741.1:n.2494T>C
|
|
|
ENST00000677624.1:c.*832T>C
|
ENSP00000503979.1:n.*832T>C
|
|
ENST00000677625.1:c.1358T>C
|
ENSP00000502857.1:p.Phe453Ser
|
|
ENST00000677856.1:n.1665T>C
|
|
|
ENST00000677915.1:c.*309T>C
|
ENSP00000503118.1:n.*309T>C
|
|
ENST00000678533.1:c.*966T>C
|
ENSP00000503873.1:n.*966T>C
|
|
ENST00000678592.1:c.*352T>C
|
ENSP00000504424.1:n.*352T>C
|
|
ENST00000278407.8:c.1412T>C
|
ENSP00000278407.4:p.Phe471Ser
|
|
ENST00000340687.10:c.1301T>C
|
ENSP00000341861.6:p.Phe434Ser
|
|
ENST00000378323.8:c.1427T>C
|
ENSP00000367574.4:p.Phe476Ser
|
|
ENST00000378324.6:c.1256T>C
|
ENSP00000367575.2:p.Phe419Ser
|
|
ENST00000403558.1:c.1541T>C
|
ENSP00000384420.1:p.Phe514Ser
|
|
ENST00000528996.1:c.613T>C
|
ENSP00000431226.1:n.613T>C
|
|
ENST00000530113.1:n.869T>C
|
|
|
ENST00000531133.5:c.913T>C
|
ENSP00000435431.1:n.913T>C
|
|
ENST00000531797.5:c.*437T>C
|
ENSP00000432554.1:n.*437T>C
|
|
ENST00000619430.1:c.543T>C
|
ENSP00000478572.1:n.543T>C
|
|
NM_000062.2:c.1412T>C , LRG_105t1:c.1412T>C
|
NP_000053.2:p.Phe471Ser
|
|
NM_001032295.1:c.1412T>C
|
NP_001027466.1:p.Phe471Ser
|
|
NM_000062.3:c.1412T>C
MANE Select
|
NP_000053.2:p.Phe471Ser
|
|
NM_001032295.2:c.1412T>C
|
NP_001027466.1:p.Phe471Ser
|
|