ENST00000460843.6:c.2885A>T
MANE Select
|
ENSP00000417980.1:p.Asp962Val
|
|
ENST00000636027.1:c.2771A>T
|
ENSP00000489961.1:p.Asp924Val
|
|
ENST00000637161.1:c.2792A>T
|
ENSP00000490328.1:p.Asp931Val
|
|
ENST00000637261.1:c.2925A>T
|
ENSP00000490815.1:n.2925A>T
|
|
ENST00000637891.1:c.779A>T
|
ENSP00000490907.1:p.Asp260Val
|
|
ENST00000460843.5:c.2885A>T
|
ENSP00000417980.1:p.Asp962Val
|
|
ENST00000462942.3:c.1742A>T
|
ENSP00000436107.1:p.Asp581Val
|
|
ENST00000486164.5:c.572A>T
|
|
|
ENST00000488242.2:n.411A>T
|
|
|
NM_024757.4:c.2885A>T
|
NP_079033.4:p.Asp962Val
|
|
XM_005266105.3:c.2876A>T
|
XP_005266162.1:p.Asp959Val
|
|
XM_005266110.1:c.2792A>T
|
XP_005266167.1:p.Asp931Val
|
|
XM_006717288.2:c.2867A>T
|
XP_006717351.1:p.Asp956Val
|
|
XM_011519021.1:c.2894A>T
|
XP_011517323.1:p.Asp965Val
|
|
XM_011519022.1:c.2891A>T
|
XP_011517324.1:p.Asp964Val
|
|
XM_011519023.1:c.2873A>T
|
XP_011517325.1:p.Asp958Val
|
|
XM_011519024.1:c.2816A>T
|
XP_011517326.1:p.Asp939Val
|
|
XM_011519025.1:c.2792A>T
|
XP_011517327.1:p.Asp931Val
|
|
XM_011519026.1:c.2750A>T
|
XP_011517328.1:p.Asp917Val
|
|
XM_011519029.1:c.1316A>T
|
XP_011517331.1:p.Asp439Val
|
|
XM_011519030.1:c.668A>T
|
XP_011517332.1:p.Asp223Val
|
|
XM_011519031.1:c.455A>T
|
XP_011517333.1:p.Asp152Val
|
|
XM_011519032.1:c.455A>T
|
XP_011517334.1:p.Asp152Val
|
|
XM_011519033.1:c.2729A>T
|
XP_011517335.1:p.Asp910Val
|
|
NM_001354263.1:c.2864A>T
|
NP_001341192.1:p.Asp955Val
|
|
XM_005266105.5:c.2876A>T
|
XP_005266162.1:p.Asp959Val
|
|
XM_011519021.3:c.2894A>T
|
XP_011517323.1:p.Asp965Val
|
|
XM_011519022.3:c.2891A>T
|
XP_011517324.1:p.Asp964Val
|
|
XM_011519023.3:c.2873A>T
|
XP_011517325.1:p.Asp958Val
|
|
XM_011519029.3:c.1316A>T
|
XP_011517331.1:p.Asp439Val
|
|
XM_011519030.3:c.668A>T
|
XP_011517332.1:p.Asp223Val
|
|
XM_017015134.1:c.2870A>T
|
XP_016870623.1:p.Asp957Val
|
|
XM_017015136.2:c.2786A>T
|
XP_016870625.1:p.Asp929Val
|
|
XM_017015137.1:c.2771A>T
|
XP_016870626.1:p.Asp924Val
|
|
XM_017015138.1:c.2771A>T
|
XP_016870627.1:p.Asp924Val
|
|
XM_024447674.1:c.2714A>T
|
XP_024303442.1:p.Asp905Val
|
|
XM_024447675.1:c.2648A>T
|
XP_024303443.1:p.Asp883Val
|
|
XM_024447676.1:c.2009A>T
|
XP_024303444.1:p.Asp670Val
|
|
XM_024447677.1:c.2009A>T
|
XP_024303445.1:p.Asp670Val
|
|
XM_024447680.1:c.2627A>T
|
XP_024303448.1:p.Asp876Val
|
|
NM_024757.5:c.2885A>T
MANE Select
|
NP_079033.4:p.Asp962Val
|
|
NM_001354263.2:c.2864A>T
|
NP_001341192.1:p.Asp955Val
|
|