ENST00000368666.7:c.266C>T
MANE Select
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ENSP00000357655.4:p.Ala89Val
|
|
ENST00000639360.1:c.170C>T
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ENSP00000491774.1:p.Ala57Val
|
|
ENST00000230529.9:c.266C>T
|
ENSP00000230529.5:p.Ala89Val
|
|
ENST00000361714.5:c.266C>T
|
ENSP00000354734.2:p.Ala89Val
|
|
ENST00000368663.4:c.266C>T
|
ENSP00000357652.4:p.Ala89Val
|
|
ENST00000368664.7:c.320C>T
|
ENSP00000357653.3:p.Ala107Val
|
|
ENST00000368666.6:c.320C>T
|
ENSP00000357655.3:p.Ala107Val
|
|
ENST00000409166.5:c.-507-71C>T
|
ENSP00000386467.1:n.-507-71C>T
|
|
ENST00000454589.5:c.266C>T
|
ENSP00000395928.1:p.Ala89Val
|
|
ENST00000604763.5:c.266C>T
|
ENSP00000473777.1:p.Ala89Val
|
|
ENST00000620524.3:n.200C>T
|
|
|
NM_003880.3:c.266C>T
|
NP_003871.1:p.Ala89Val
|
|
NM_198239.1:c.320C>T
|
NP_937882.1:p.Ala107Val
|
|
NR_125353.1:n.456C>T
|
|
|
NR_125354.1:n.376C>T
|
|
|
XM_011536220.1:c.266C>T
|
XP_011534522.1:p.Ala89Val
|
|
XM_011536221.1:c.329C>T
|
XP_011534523.1:p.Ala110Val
|
|
XM_011536222.1:c.404C>T
|
XP_011534524.1:p.Ala135Val
|
|
XM_011536222.2:c.329C>T
|
XP_011534524.2:p.Ala110Val
|
|
XR_001743705.1:n.804C>T
|
|
|
NM_003880.4:c.266C>T
|
NP_003871.1:p.Ala89Val
|
|
NM_198239.2:c.266C>T
MANE Select
|
NP_937882.2:p.Ala89Val
|
|
NR_125353.2:n.520C>T
|
|
|
NR_125354.3:n.347C>T
|
|
|