ENST00000460843.6:c.2988G>A
MANE Select
|
ENSP00000417980.1:p.Gln996=
|
|
ENST00000636027.1:c.2874G>A
|
ENSP00000489961.1:p.Gln958=
|
|
ENST00000637161.1:c.2895G>A
|
ENSP00000490328.1:p.Gln965=
|
|
ENST00000637261.1:c.3028G>A
|
ENSP00000490815.1:n.3028G>A
|
|
ENST00000637891.1:c.882G>A
|
ENSP00000490907.1:p.Gln294=
|
|
ENST00000460843.5:c.2988G>A
|
ENSP00000417980.1:p.Gln996=
|
|
ENST00000462942.3:c.1845G>A
|
ENSP00000436107.1:p.Gln615=
|
|
ENST00000486164.5:c.675G>A
|
|
|
ENST00000488242.2:n.514G>A
|
|
|
NM_024757.4:c.2988G>A
|
NP_079033.4:p.Gln996=
|
|
XM_005266105.3:c.2979G>A
|
XP_005266162.1:p.Gln993=
|
|
XM_005266110.1:c.2895G>A
|
XP_005266167.1:p.Gln965=
|
|
XM_006717288.2:c.2970G>A
|
XP_006717351.1:p.Gln990=
|
|
XM_011519021.1:c.2997G>A
|
XP_011517323.1:p.Gln999=
|
|
XM_011519022.1:c.2994G>A
|
XP_011517324.1:p.Gln998=
|
|
XM_011519023.1:c.2976G>A
|
XP_011517325.1:p.Gln992=
|
|
XM_011519024.1:c.2919G>A
|
XP_011517326.1:p.Gln973=
|
|
XM_011519025.1:c.2895G>A
|
XP_011517327.1:p.Gln965=
|
|
XM_011519026.1:c.2853G>A
|
XP_011517328.1:p.Gln951=
|
|
XM_011519029.1:c.1419G>A
|
XP_011517331.1:p.Gln473=
|
|
XM_011519030.1:c.771G>A
|
XP_011517332.1:p.Gln257=
|
|
XM_011519031.1:c.558G>A
|
XP_011517333.1:p.Gln186=
|
|
XM_011519032.1:c.558G>A
|
XP_011517334.1:p.Gln186=
|
|
XM_011519033.1:c.2832G>A
|
XP_011517335.1:p.Gln944=
|
|
NM_001354263.1:c.2967G>A
|
NP_001341192.1:p.Gln989=
|
|
XM_005266105.5:c.2979G>A
|
XP_005266162.1:p.Gln993=
|
|
XM_011519021.3:c.2997G>A
|
XP_011517323.1:p.Gln999=
|
|
XM_011519022.3:c.2994G>A
|
XP_011517324.1:p.Gln998=
|
|
XM_011519023.3:c.2976G>A
|
XP_011517325.1:p.Gln992=
|
|
XM_011519029.3:c.1419G>A
|
XP_011517331.1:p.Gln473=
|
|
XM_011519030.3:c.771G>A
|
XP_011517332.1:p.Gln257=
|
|
XM_017015134.1:c.2973G>A
|
XP_016870623.1:p.Gln991=
|
|
XM_017015136.2:c.2889G>A
|
XP_016870625.1:p.Gln963=
|
|
XM_017015137.1:c.2874G>A
|
XP_016870626.1:p.Gln958=
|
|
XM_017015138.1:c.2874G>A
|
XP_016870627.1:p.Gln958=
|
|
XM_024447674.1:c.2817G>A
|
XP_024303442.1:p.Gln939=
|
|
XM_024447675.1:c.2751G>A
|
XP_024303443.1:p.Gln917=
|
|
XM_024447676.1:c.2112G>A
|
XP_024303444.1:p.Gln704=
|
|
XM_024447677.1:c.2112G>A
|
XP_024303445.1:p.Gln704=
|
|
XM_024447680.1:c.2730G>A
|
XP_024303448.1:p.Gln910=
|
|
NM_024757.5:c.2988G>A
MANE Select
|
NP_079033.4:p.Gln996=
|
|
NM_001354263.2:c.2967G>A
|
NP_001341192.1:p.Gln989=
|
|