ENST00000234071.8:c.613G>A
MANE Select
|
ENSP00000234071.4:p.Glu205Lys
|
|
ENST00000234071.7:c.613G>A
|
ENSP00000234071.3:p.Glu205Lys
|
|
ENST00000402125.2:c.121-2195G>A
|
|
|
ENST00000409048.1:c.715G>A
|
ENSP00000386679.1:p.Glu239Lys
|
|
ENST00000464089.1:n.199G>A
|
|
|
NM_000312.3:c.613G>A , LRG_599t1:c.613G>A
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NP_000303.1:p.Glu205Lys
|
|
XM_005263715.3:c.796G>A
|
XP_005263772.1:p.Glu266Lys
|
|
XM_005263716.3:c.778G>A
|
XP_005263773.1:p.Glu260Lys
|
|
XM_005263717.3:c.676G>A
|
XP_005263774.1:p.Glu226Lys
|
|
XM_005263717.4:c.676G>A
|
XP_005263774.1:p.Glu226Lys
|
|
XM_017004505.1:c.856G>A
|
XP_016859994.1:p.Glu286Lys
|
|
XM_024453002.1:c.958G>A
|
XP_024308770.1:p.Glu320Lys
|
|
XM_024453003.1:c.898G>A
|
XP_024308771.1:p.Glu300Lys
|
|
XM_024453004.1:c.796G>A
|
XP_024308772.1:p.Glu266Lys
|
|
XM_024453005.1:c.778G>A
|
XP_024308773.1:p.Glu260Lys
|
|
XM_024453006.1:c.715G>A
|
XP_024308774.1:p.Glu239Lys
|
|
XR_923313.2:n.4423C>T
|
|
|
NM_000312.4:c.613G>A
MANE Select
|
NP_000303.1:p.Glu205Lys
|
|
NM_001375602.1:c.796G>A
|
NP_001362531.1:p.Glu266Lys
|
|
NM_001375603.1:c.778G>A
|
NP_001362532.1:p.Glu260Lys
|
|
NM_001375604.1:c.676G>A
|
NP_001362533.1:p.Glu226Lys
|
|
NM_001375605.1:c.715G>A
|
NP_001362534.1:p.Glu239Lys
|
|
NM_001375606.1:c.781G>A
|
NP_001362535.1:p.Glu261Lys
|
|
NM_001375607.1:c.799G>A
|
NP_001362536.1:p.Glu267Lys
|
|
NM_001375608.1:c.556G>A
|
NP_001362537.1:p.Glu186Lys
|
|
NM_001375609.1:c.589G>A
|
NP_001362538.1:p.Glu197Lys
|
|
NM_001375610.1:c.607G>A
|
NP_001362539.1:p.Glu203Lys
|
|
NM_001375611.1:c.613G>A
|
NP_001362540.1:p.Glu205Lys
|
|
NM_001375613.1:c.613G>A
|
NP_001362542.1:p.Glu205Lys
|
|