ENST00000682114.1:c.409G>T
|
ENSP00000507245.1:p.Asp137Tyr
|
|
ENST00000682478.1:n.599G>T
|
|
|
ENST00000683576.1:n.599G>T
|
|
|
ENST00000683627.1:c.409G>T
|
ENSP00000507533.1:p.Asp137Tyr
|
|
ENST00000684082.1:c.366G>T
|
ENSP00000508266.1:n.366G>T
|
|
ENST00000684633.1:n.381G>T
|
|
|
ENST00000684678.1:c.405G>T
|
ENSP00000507059.1:n.405G>T
|
|
ENST00000369842.9:c.409G>T
MANE Select
|
ENSP00000358857.4:p.Asp137Tyr
|
|
ENST00000369835.3:c.304G>T
|
ENSP00000358850.3:p.Asp102Tyr
|
|
ENST00000369842.8:c.409G>T
|
ENSP00000358857.4:p.Asp137Tyr
|
|
ENST00000428228.5:c.*314G>T
|
ENSP00000401081.1:n.*314G>T
|
|
ENST00000468294.5:n.369G>T
|
|
|
ENST00000471965.1:n.198G>T
|
|
|
ENST00000485261.1:n.599G>T
|
|
|
ENST00000486738.5:n.767G>T
|
|
|
ENST00000492448.1:n.392G>T
|
|
|
NM_000117.2:c.409G>T , LRG_745t1:c.409G>T
|
NP_000108.1:p.Asp137Tyr
|
|
XM_024452349.1:c.415G>T
|
XP_024308117.1:p.Asp139Tyr
|
|
NM_000117.3:c.409G>T
MANE Select
|
NP_000108.1:p.Asp137Tyr
|
|