ENST00000460843.6:c.2617G>T
MANE Select
|
ENSP00000417980.1:p.Gly873Cys
|
|
ENST00000636027.1:c.2503G>T
|
ENSP00000489961.1:p.Gly835Cys
|
|
ENST00000637161.1:c.2524G>T
|
ENSP00000490328.1:p.Gly842Cys
|
|
ENST00000637261.1:c.2657G>T
|
ENSP00000490815.1:n.2657G>T
|
|
ENST00000637891.1:c.511G>T
|
ENSP00000490907.1:p.Gly171Cys
|
|
ENST00000637949.1:c.295G>T
|
ENSP00000489786.1:p.Gly99Cys
|
|
ENST00000460843.5:c.2617G>T
|
ENSP00000417980.1:p.Gly873Cys
|
|
ENST00000462942.3:c.1474G>T
|
ENSP00000436107.1:p.Gly492Cys
|
|
ENST00000482340.5:c.187G>T
|
ENSP00000486748.1:p.Gly63Cys
|
|
ENST00000486164.5:c.195G>T
|
|
|
ENST00000488242.2:n.143G>T
|
|
|
ENST00000493484.5:c.187G>T
|
ENSP00000486503.1:p.Gly63Cys
|
|
NM_024757.4:c.2617G>T
|
NP_079033.4:p.Gly873Cys
|
|
XM_005266105.3:c.2608G>T
|
XP_005266162.1:p.Gly870Cys
|
|
XM_005266110.1:c.2524G>T
|
XP_005266167.1:p.Gly842Cys
|
|
XM_006717288.2:c.2599G>T
|
XP_006717351.1:p.Gly867Cys
|
|
XM_011519021.1:c.2626G>T
|
XP_011517323.1:p.Gly876Cys
|
|
XM_011519022.1:c.2623G>T
|
XP_011517324.1:p.Gly875Cys
|
|
XM_011519023.1:c.2605G>T
|
XP_011517325.1:p.Gly869Cys
|
|
XM_011519024.1:c.2548G>T
|
XP_011517326.1:p.Gly850Cys
|
|
XM_011519025.1:c.2524G>T
|
XP_011517327.1:p.Gly842Cys
|
|
XM_011519026.1:c.2482G>T
|
XP_011517328.1:p.Gly828Cys
|
|
XM_011519027.1:c.2626G>T
|
XP_011517329.1:p.Gly876Cys
|
|
XM_011519029.1:c.1048G>T
|
XP_011517331.1:p.Gly350Cys
|
|
XM_011519030.1:c.400G>T
|
XP_011517332.1:p.Gly134Cys
|
|
XM_011519031.1:c.187G>T
|
XP_011517333.1:p.Gly63Cys
|
|
XM_011519032.1:c.187G>T
|
XP_011517334.1:p.Gly63Cys
|
|
XM_011519033.1:c.2461G>T
|
XP_011517335.1:p.Gly821Cys
|
|
NM_001354263.1:c.2596G>T
|
NP_001341192.1:p.Gly866Cys
|
|
XM_005266105.5:c.2608G>T
|
XP_005266162.1:p.Gly870Cys
|
|
XM_011519021.3:c.2626G>T
|
XP_011517323.1:p.Gly876Cys
|
|
XM_011519022.3:c.2623G>T
|
XP_011517324.1:p.Gly875Cys
|
|
XM_011519023.3:c.2605G>T
|
XP_011517325.1:p.Gly869Cys
|
|
XM_011519029.3:c.1048G>T
|
XP_011517331.1:p.Gly350Cys
|
|
XM_011519030.3:c.400G>T
|
XP_011517332.1:p.Gly134Cys
|
|
XM_017015134.1:c.2602G>T
|
XP_016870623.1:p.Gly868Cys
|
|
XM_017015136.2:c.2518G>T
|
XP_016870625.1:p.Gly840Cys
|
|
XM_017015137.1:c.2503G>T
|
XP_016870626.1:p.Gly835Cys
|
|
XM_017015138.1:c.2503G>T
|
XP_016870627.1:p.Gly835Cys
|
|
XM_024447674.1:c.2446G>T
|
XP_024303442.1:p.Gly816Cys
|
|
XM_024447675.1:c.2380G>T
|
XP_024303443.1:p.Gly794Cys
|
|
XM_024447676.1:c.1741G>T
|
XP_024303444.1:p.Gly581Cys
|
|
XM_024447677.1:c.1741G>T
|
XP_024303445.1:p.Gly581Cys
|
|
XM_024447678.1:c.2524G>T
|
XP_024303446.1:p.Gly842Cys
|
|
XM_024447680.1:c.2359G>T
|
XP_024303448.1:p.Gly787Cys
|
|
NM_024757.5:c.2617G>T
MANE Select
|
NP_079033.4:p.Gly873Cys
|
|
NM_001354263.2:c.2596G>T
|
NP_001341192.1:p.Gly866Cys
|
|