ENST00000460843.6:c.2921C>A
MANE Select
|
ENSP00000417980.1:p.Thr974Lys
|
|
ENST00000636027.1:c.2807C>A
|
ENSP00000489961.1:p.Thr936Lys
|
|
ENST00000637161.1:c.2828C>A
|
ENSP00000490328.1:p.Thr943Lys
|
|
ENST00000637261.1:c.2961C>A
|
ENSP00000490815.1:n.2961C>A
|
|
ENST00000637891.1:c.815C>A
|
ENSP00000490907.1:p.Thr272Lys
|
|
ENST00000460843.5:c.2921C>A
|
ENSP00000417980.1:p.Thr974Lys
|
|
ENST00000462942.3:c.1778C>A
|
ENSP00000436107.1:p.Thr593Lys
|
|
ENST00000486164.5:c.608C>A
|
|
|
ENST00000488242.2:n.447C>A
|
|
|
NM_024757.4:c.2921C>A
|
NP_079033.4:p.Thr974Lys
|
|
XM_005266105.3:c.2912C>A
|
XP_005266162.1:p.Thr971Lys
|
|
XM_005266110.1:c.2828C>A
|
XP_005266167.1:p.Thr943Lys
|
|
XM_006717288.2:c.2903C>A
|
XP_006717351.1:p.Thr968Lys
|
|
XM_011519021.1:c.2930C>A
|
XP_011517323.1:p.Thr977Lys
|
|
XM_011519022.1:c.2927C>A
|
XP_011517324.1:p.Thr976Lys
|
|
XM_011519023.1:c.2909C>A
|
XP_011517325.1:p.Thr970Lys
|
|
XM_011519024.1:c.2852C>A
|
XP_011517326.1:p.Thr951Lys
|
|
XM_011519025.1:c.2828C>A
|
XP_011517327.1:p.Thr943Lys
|
|
XM_011519026.1:c.2786C>A
|
XP_011517328.1:p.Thr929Lys
|
|
XM_011519029.1:c.1352C>A
|
XP_011517331.1:p.Thr451Lys
|
|
XM_011519030.1:c.704C>A
|
XP_011517332.1:p.Thr235Lys
|
|
XM_011519031.1:c.491C>A
|
XP_011517333.1:p.Thr164Lys
|
|
XM_011519032.1:c.491C>A
|
XP_011517334.1:p.Thr164Lys
|
|
XM_011519033.1:c.2765C>A
|
XP_011517335.1:p.Thr922Lys
|
|
NM_001354263.1:c.2900C>A
|
NP_001341192.1:p.Thr967Lys
|
|
XM_005266105.5:c.2912C>A
|
XP_005266162.1:p.Thr971Lys
|
|
XM_011519021.3:c.2930C>A
|
XP_011517323.1:p.Thr977Lys
|
|
XM_011519022.3:c.2927C>A
|
XP_011517324.1:p.Thr976Lys
|
|
XM_011519023.3:c.2909C>A
|
XP_011517325.1:p.Thr970Lys
|
|
XM_011519029.3:c.1352C>A
|
XP_011517331.1:p.Thr451Lys
|
|
XM_011519030.3:c.704C>A
|
XP_011517332.1:p.Thr235Lys
|
|
XM_017015134.1:c.2906C>A
|
XP_016870623.1:p.Thr969Lys
|
|
XM_017015136.2:c.2822C>A
|
XP_016870625.1:p.Thr941Lys
|
|
XM_017015137.1:c.2807C>A
|
XP_016870626.1:p.Thr936Lys
|
|
XM_017015138.1:c.2807C>A
|
XP_016870627.1:p.Thr936Lys
|
|
XM_024447674.1:c.2750C>A
|
XP_024303442.1:p.Thr917Lys
|
|
XM_024447675.1:c.2684C>A
|
XP_024303443.1:p.Thr895Lys
|
|
XM_024447676.1:c.2045C>A
|
XP_024303444.1:p.Thr682Lys
|
|
XM_024447677.1:c.2045C>A
|
XP_024303445.1:p.Thr682Lys
|
|
XM_024447680.1:c.2663C>A
|
XP_024303448.1:p.Thr888Lys
|
|
NM_024757.5:c.2921C>A
MANE Select
|
NP_079033.4:p.Thr974Lys
|
|
NM_001354263.2:c.2900C>A
|
NP_001341192.1:p.Thr967Lys
|
|