ENST00000361420.8:c.2314A>G
MANE Select
|
ENSP00000355010.3:p.Ile772Val
|
|
ENST00000370903.8:c.2329A>G
|
ENSP00000359940.3:p.Ile777Val
|
|
ENST00000651402.1:c.10-2985A>G
|
|
|
ENST00000651526.1:n.716A>G
|
|
|
ENST00000651556.1:c.2314A>G
|
ENSP00000498789.1:p.Ile772Val
|
|
ENST00000652189.1:c.2314A>G
|
ENSP00000498607.1:p.Ile772Val
|
|
ENST00000361420.7:c.2314A>G
|
ENSP00000355010.3:p.Ile772Val
|
|
ENST00000370903.7:c.2329A>G
|
ENSP00000359940.3:p.Ile777Val
|
|
ENST00000370904.6:c.2287A>G
|
ENSP00000359941.1:p.Ile763Val
|
|
ENST00000370910.5:c.2287A>G
|
ENSP00000359947.1:p.Ile763Val
|
|
NM_001170961.1:c.2329A>G
|
NP_001164432.1:p.Ile777Val
|
|
NM_001170962.1:c.2287A>G
|
NP_001164433.1:p.Ile763Val
|
|
NM_001555.4:c.2314A>G
|
NP_001546.2:p.Ile772Val
|
|
XM_011531330.1:c.2329A>G
|
XP_011529632.1:p.Ile777Val
|
|
XM_011531331.1:c.2329A>G
|
XP_011529633.1:p.Ile777Val
|
|
XM_011531332.1:c.2329A>G
|
XP_011529634.1:p.Ile777Val
|
|
XM_011531333.1:c.2329A>G
|
XP_011529635.1:p.Ile777Val
|
|
XM_011531334.1:c.2329A>G
|
XP_011529636.1:p.Ile777Val
|
|
XM_011531335.1:c.556A>G
|
XP_011529637.1:p.Ile186Val
|
|
XM_011531333.2:c.2329A>G
|
XP_011529635.1:p.Ile777Val
|
|
XM_011531334.2:c.2329A>G
|
XP_011529636.1:p.Ile777Val
|
|
NM_001555.5:c.2314A>G
MANE Select
|
NP_001546.2:p.Ile772Val
|
|
NM_001170962.2:c.2287A>G
|
NP_001164433.1:p.Ile763Val
|
|
NM_001170961.2:c.2329A>G
|
NP_001164432.1:p.Ile777Val
|
|