ENST00000599672.6:c.259A>G
MANE Select
|
ENSP00000470560.1:p.Ile87Val
|
|
ENST00000261406.7:c.241A>G
|
ENSP00000476966.2:p.Ile81Val
|
|
ENST00000539196.2:c.122A>G
|
|
|
ENST00000599672.5:c.259A>G
|
ENSP00000470560.1:p.Ile87Val
|
|
ENST00000607161.5:c.262A>G
|
ENSP00000480420.1:p.Ile88Val
|
|
ENST00000611981.1:n.270A>G
|
|
|
ENST00000620255.1:n.248A>G
|
|
|
NM_006331.7:c.259A>G
|
NP_006322.4:p.Ile87Val
|
|
XM_011520907.1:c.259A>G
|
XP_011519209.1:p.Ile87Val
|
|
NM_001320049.1:c.259A>G
|
NP_001306978.1:p.Ile87Val
|
|
NR_135131.1:n.402A>G
|
|
|
NM_006331.8:c.259A>G
MANE Select
|
NP_006322.4:p.Ile87Val
|
|
NM_001320049.2:c.259A>G
|
NP_001306978.1:p.Ile87Val
|
|
NR_135131.2:n.270A>G
|
|
|