ENST00000460843.6:c.2920A>T
MANE Select
|
ENSP00000417980.1:p.Thr974Ser
|
|
ENST00000636027.1:c.2806A>T
|
ENSP00000489961.1:p.Thr936Ser
|
|
ENST00000637161.1:c.2827A>T
|
ENSP00000490328.1:p.Thr943Ser
|
|
ENST00000637261.1:c.2960A>T
|
ENSP00000490815.1:n.2960A>T
|
|
ENST00000637891.1:c.814A>T
|
ENSP00000490907.1:p.Thr272Ser
|
|
ENST00000460843.5:c.2920A>T
|
ENSP00000417980.1:p.Thr974Ser
|
|
ENST00000462942.3:c.1777A>T
|
ENSP00000436107.1:p.Thr593Ser
|
|
ENST00000486164.5:c.607A>T
|
|
|
ENST00000488242.2:n.446A>T
|
|
|
NM_024757.4:c.2920A>T
|
NP_079033.4:p.Thr974Ser
|
|
XM_005266105.3:c.2911A>T
|
XP_005266162.1:p.Thr971Ser
|
|
XM_005266110.1:c.2827A>T
|
XP_005266167.1:p.Thr943Ser
|
|
XM_006717288.2:c.2902A>T
|
XP_006717351.1:p.Thr968Ser
|
|
XM_011519021.1:c.2929A>T
|
XP_011517323.1:p.Thr977Ser
|
|
XM_011519022.1:c.2926A>T
|
XP_011517324.1:p.Thr976Ser
|
|
XM_011519023.1:c.2908A>T
|
XP_011517325.1:p.Thr970Ser
|
|
XM_011519024.1:c.2851A>T
|
XP_011517326.1:p.Thr951Ser
|
|
XM_011519025.1:c.2827A>T
|
XP_011517327.1:p.Thr943Ser
|
|
XM_011519026.1:c.2785A>T
|
XP_011517328.1:p.Thr929Ser
|
|
XM_011519029.1:c.1351A>T
|
XP_011517331.1:p.Thr451Ser
|
|
XM_011519030.1:c.703A>T
|
XP_011517332.1:p.Thr235Ser
|
|
XM_011519031.1:c.490A>T
|
XP_011517333.1:p.Thr164Ser
|
|
XM_011519032.1:c.490A>T
|
XP_011517334.1:p.Thr164Ser
|
|
XM_011519033.1:c.2764A>T
|
XP_011517335.1:p.Thr922Ser
|
|
NM_001354263.1:c.2899A>T
|
NP_001341192.1:p.Thr967Ser
|
|
XM_005266105.5:c.2911A>T
|
XP_005266162.1:p.Thr971Ser
|
|
XM_011519021.3:c.2929A>T
|
XP_011517323.1:p.Thr977Ser
|
|
XM_011519022.3:c.2926A>T
|
XP_011517324.1:p.Thr976Ser
|
|
XM_011519023.3:c.2908A>T
|
XP_011517325.1:p.Thr970Ser
|
|
XM_011519029.3:c.1351A>T
|
XP_011517331.1:p.Thr451Ser
|
|
XM_011519030.3:c.703A>T
|
XP_011517332.1:p.Thr235Ser
|
|
XM_017015134.1:c.2905A>T
|
XP_016870623.1:p.Thr969Ser
|
|
XM_017015136.2:c.2821A>T
|
XP_016870625.1:p.Thr941Ser
|
|
XM_017015137.1:c.2806A>T
|
XP_016870626.1:p.Thr936Ser
|
|
XM_017015138.1:c.2806A>T
|
XP_016870627.1:p.Thr936Ser
|
|
XM_024447674.1:c.2749A>T
|
XP_024303442.1:p.Thr917Ser
|
|
XM_024447675.1:c.2683A>T
|
XP_024303443.1:p.Thr895Ser
|
|
XM_024447676.1:c.2044A>T
|
XP_024303444.1:p.Thr682Ser
|
|
XM_024447677.1:c.2044A>T
|
XP_024303445.1:p.Thr682Ser
|
|
XM_024447680.1:c.2662A>T
|
XP_024303448.1:p.Thr888Ser
|
|
NM_024757.5:c.2920A>T
MANE Select
|
NP_079033.4:p.Thr974Ser
|
|
NM_001354263.2:c.2899A>T
|
NP_001341192.1:p.Thr967Ser
|
|