ENST00000336079.8:c.1136T>C
MANE Select
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ENSP00000336725.3:p.Phe379Ser
|
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ENST00000336079.7:c.1136T>C
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ENSP00000336725.3:p.Phe379Ser
|
|
ENST00000360160.8:c.1136T>C
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ENSP00000353284.4:p.Phe379Ser
|
|
ENST00000495478.1:n.251T>C
|
|
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NM_001122665.2:c.1136T>C
|
NP_001116137.1:p.Phe379Ser
|
|
NM_001302552.1:c.1127T>C
|
NP_001289481.1:p.Phe376Ser
|
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NM_004660.4:c.1136T>C
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NP_004651.2:p.Phe379Ser
|
|
XM_006724878.1:c.1136T>C
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XP_006724941.1:p.Phe379Ser
|
|
XM_011531471.1:c.1136T>C
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XP_011529773.1:p.Phe379Ser
|
|
NM_001122665.3:c.1136T>C
|
NP_001116137.1:p.Phe379Ser
|
|
NM_001302552.2:c.1127T>C
|
NP_001289481.1:p.Phe376Ser
|
|
NM_001324195.1:c.1136T>C
|
NP_001311124.1:p.Phe379Ser
|
|
NR_136716.1:n.1605T>C
|
|
|
NR_136717.1:n.1367T>C
|
|
|
NR_136718.1:n.1685T>C
|
|
|
NR_136719.1:n.1475T>C
|
|
|
NR_136720.1:n.1605T>C
|
|
|
NR_136721.1:n.1198T>C
|
|
|
NR_136722.1:n.1282T>C
|
|
|
NR_136723.1:n.1600T>C
|
|
|
NR_136724.1:n.1520T>C
|
|
|
XR_001756014.2:n.1240T>C
|
|
|
NM_004660.5:c.1136T>C
MANE Select
|
NP_004651.2:p.Phe379Ser
|
|
NM_001302552.3:c.1127T>C
|
NP_001289481.1:p.Phe376Ser
|
|
NM_001324195.2:c.1136T>C
|
NP_001311124.1:p.Phe379Ser
|
|
NR_136716.2:n.1523T>C
|
|
|
NR_136717.2:n.1285T>C
|
|
|
NR_136718.2:n.1603T>C
|
|
|
NR_136719.2:n.1393T>C
|
|
|
NR_136720.2:n.1523T>C
|
|
|
NR_136721.2:n.1188T>C
|
|
|