ENST00000460843.6:c.3021G>C
MANE Select
|
ENSP00000417980.1:p.Glu1007Asp
|
|
ENST00000636027.1:c.2907G>C
|
ENSP00000489961.1:p.Glu969Asp
|
|
ENST00000637161.1:c.2928G>C
|
ENSP00000490328.1:p.Glu976Asp
|
|
ENST00000637261.1:c.3061G>C
|
ENSP00000490815.1:n.3061G>C
|
|
ENST00000637891.1:c.915G>C
|
ENSP00000490907.1:p.Glu305Asp
|
|
ENST00000460843.5:c.3021G>C
|
ENSP00000417980.1:p.Glu1007Asp
|
|
ENST00000462942.3:c.1878G>C
|
ENSP00000436107.1:p.Glu626Asp
|
|
ENST00000486164.5:c.708G>C
|
|
|
ENST00000488242.2:n.547G>C
|
|
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NM_024757.4:c.3021G>C
|
NP_079033.4:p.Glu1007Asp
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|
XM_005266105.3:c.3012G>C
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XP_005266162.1:p.Glu1004Asp
|
|
XM_005266110.1:c.2928G>C
|
XP_005266167.1:p.Glu976Asp
|
|
XM_006717288.2:c.3003G>C
|
XP_006717351.1:p.Glu1001Asp
|
|
XM_011519021.1:c.3030G>C
|
XP_011517323.1:p.Glu1010Asp
|
|
XM_011519022.1:c.3027G>C
|
XP_011517324.1:p.Glu1009Asp
|
|
XM_011519023.1:c.3009G>C
|
XP_011517325.1:p.Glu1003Asp
|
|
XM_011519024.1:c.2952G>C
|
XP_011517326.1:p.Glu984Asp
|
|
XM_011519025.1:c.2928G>C
|
XP_011517327.1:p.Glu976Asp
|
|
XM_011519026.1:c.2886G>C
|
XP_011517328.1:p.Glu962Asp
|
|
XM_011519029.1:c.1452G>C
|
XP_011517331.1:p.Glu484Asp
|
|
XM_011519030.1:c.804G>C
|
XP_011517332.1:p.Glu268Asp
|
|
XM_011519031.1:c.591G>C
|
XP_011517333.1:p.Glu197Asp
|
|
XM_011519032.1:c.591G>C
|
XP_011517334.1:p.Glu197Asp
|
|
XM_011519033.1:c.2865G>C
|
XP_011517335.1:p.Glu955Asp
|
|
NM_001354263.1:c.3000G>C
|
NP_001341192.1:p.Glu1000Asp
|
|
XM_005266105.5:c.3012G>C
|
XP_005266162.1:p.Glu1004Asp
|
|
XM_011519021.3:c.3030G>C
|
XP_011517323.1:p.Glu1010Asp
|
|
XM_011519022.3:c.3027G>C
|
XP_011517324.1:p.Glu1009Asp
|
|
XM_011519023.3:c.3009G>C
|
XP_011517325.1:p.Glu1003Asp
|
|
XM_011519029.3:c.1452G>C
|
XP_011517331.1:p.Glu484Asp
|
|
XM_011519030.3:c.804G>C
|
XP_011517332.1:p.Glu268Asp
|
|
XM_017015134.1:c.3006G>C
|
XP_016870623.1:p.Glu1002Asp
|
|
XM_017015136.2:c.2922G>C
|
XP_016870625.1:p.Glu974Asp
|
|
XM_017015137.1:c.2907G>C
|
XP_016870626.1:p.Glu969Asp
|
|
XM_017015138.1:c.2907G>C
|
XP_016870627.1:p.Glu969Asp
|
|
XM_024447674.1:c.2850G>C
|
XP_024303442.1:p.Glu950Asp
|
|
XM_024447675.1:c.2784G>C
|
XP_024303443.1:p.Glu928Asp
|
|
XM_024447676.1:c.2145G>C
|
XP_024303444.1:p.Glu715Asp
|
|
XM_024447677.1:c.2145G>C
|
XP_024303445.1:p.Glu715Asp
|
|
XM_024447680.1:c.2763G>C
|
XP_024303448.1:p.Glu921Asp
|
|
NM_024757.5:c.3021G>C
MANE Select
|
NP_079033.4:p.Glu1007Asp
|
|
NM_001354263.2:c.3000G>C
|
NP_001341192.1:p.Glu1000Asp
|
|