|
ENST00000395105.9:c.1982G>T
MANE Select
|
ENSP00000378537.4:p.Gly661Val
|
|
|
ENST00000323940.9:c.1982G>T
|
ENSP00000326085.5:p.Gly661Val
|
|
|
ENST00000395105.8:c.1982G>T
|
ENSP00000378537.4:p.Gly661Val
|
|
|
ENST00000416286.7:c.1958G>T
|
ENSP00000400403.3:p.Gly653Val
|
|
|
ENST00000423167.6:c.1955G>T
|
ENSP00000413012.2:p.Gly652Val
|
|
|
ENST00000449139.6:c.1982G>T
|
ENSP00000410221.2:p.Gly661Val
|
|
|
ENST00000535552.5:c.2093G>T
|
ENSP00000440238.1:p.Gly698Val
|
|
|
ENST00000545137.5:n.1691G>T
|
|
|
|
ENST00000563965.5:c.2099G>T
|
ENSP00000456609.1:p.Gly700Val
|
|
|
ENST00000574278.5:c.2027G>T
|
ENSP00000458827.1:p.Gly676Val
|
|
|
ENST00000574439.5:n.2254G>T
|
|
|
|
ENST00000616000.4:c.1982G>T
|
ENSP00000479112.1:p.Gly661Val
|
|
|
NM_001142617.1:c.1982G>T
|
NP_001136089.1:p.Gly661Val
|
|
|
NM_001142618.1:c.1982G>T
|
NP_001136090.1:p.Gly661Val
|
|
|
NM_001142619.1:c.1955G>T
|
NP_001136091.1:p.Gly652Val
|
|
|
NM_001199040.1:c.2093G>T
|
NP_001185969.1:p.Gly698Val
|
|
|
NM_001199041.1:c.2027G>T
|
NP_001185970.1:p.Gly676Val
|
|
|
NM_001199042.1:c.2099G>T
|
NP_001185971.1:p.Gly700Val
|
|
|
NM_022369.3:c.1982G>T
|
NP_071764.3:p.Gly661Val
|
|
|
XM_011521883.1:c.1982G>T
|
XP_011520185.1:p.Gly661Val
|
|
|
XM_011521884.1:c.1793G>T
|
XP_011520186.1:p.Gly598Val
|
|
|
XM_017022478.1:c.2030G>T
|
XP_016877967.1:p.Gly677Val
|
|
|
XM_017022479.1:c.1982G>T
|
XP_016877968.1:p.Gly661Val
|
|
|
XM_017022480.1:c.1793G>T
|
XP_016877969.1:p.Gly598Val
|
|
|
NM_022369.4:c.1982G>T
MANE Select
|
NP_071764.3:p.Gly661Val
|
|
|
NM_001142617.2:c.1982G>T
|
NP_001136089.1:p.Gly661Val
|
|
|
NM_001142619.2:c.1955G>T
|
NP_001136091.1:p.Gly652Val
|
|
|
NM_001199042.2:c.2099G>T
|
NP_001185971.1:p.Gly700Val
|
|
|
NM_001142618.2:c.1982G>T
|
NP_001136090.1:p.Gly661Val
|
|
|
NM_001199040.2:c.2093G>T
|
NP_001185969.1:p.Gly698Val
|
|
|
NM_001199041.2:c.2027G>T
|
NP_001185970.1:p.Gly676Val
|
|
