ENST00000278407.9:c.1497G>T
MANE Select
|
ENSP00000278407.4:p.Arg499Ser
|
|
ENST00000528996.2:c.*394G>T
|
ENSP00000431226.2:n.*394G>T
|
|
ENST00000531605.2:c.*1273G>T
|
ENSP00000503752.1:n.*1273G>T
|
|
ENST00000619430.2:c.1293G>T
|
ENSP00000478572.2:p.Arg431Ser
|
|
ENST00000676670.1:c.1497G>T
|
ENSP00000504807.1:p.Arg499Ser
|
|
ENST00000676741.1:n.2579G>T
|
|
|
ENST00000677624.1:c.*917G>T
|
ENSP00000503979.1:n.*917G>T
|
|
ENST00000677625.1:c.1443G>T
|
ENSP00000502857.1:p.Arg481Ser
|
|
ENST00000677856.1:n.1750G>T
|
|
|
ENST00000677915.1:c.*394G>T
|
ENSP00000503118.1:n.*394G>T
|
|
ENST00000678533.1:c.*1051G>T
|
ENSP00000503873.1:n.*1051G>T
|
|
ENST00000678592.1:c.*437G>T
|
ENSP00000504424.1:n.*437G>T
|
|
ENST00000278407.8:c.1497G>T
|
ENSP00000278407.4:p.Arg499Ser
|
|
ENST00000340687.10:c.1386G>T
|
ENSP00000341861.6:p.Arg462Ser
|
|
ENST00000378323.8:c.1512G>T
|
ENSP00000367574.4:p.Arg504Ser
|
|
ENST00000378324.6:c.1341G>T
|
ENSP00000367575.2:p.Arg447Ser
|
|
ENST00000403558.1:c.1626G>T
|
ENSP00000384420.1:p.Arg542Ser
|
|
ENST00000528996.1:c.698G>T
|
ENSP00000431226.1:n.698G>T
|
|
ENST00000531133.5:c.998G>T
|
ENSP00000435431.1:n.998G>T
|
|
ENST00000531797.5:c.*522G>T
|
ENSP00000432554.1:n.*522G>T
|
|
ENST00000619430.1:c.628G>T
|
ENSP00000478572.1:n.628G>T
|
|
NM_000062.2:c.1497G>T , LRG_105t1:c.1497G>T
|
NP_000053.2:p.Arg499Ser
|
|
NM_001032295.1:c.1497G>T
|
NP_001027466.1:p.Arg499Ser
|
|
NM_000062.3:c.1497G>T
MANE Select
|
NP_000053.2:p.Arg499Ser
|
|
NM_001032295.2:c.1497G>T
|
NP_001027466.1:p.Arg499Ser
|
|