ENST00000460843.6:c.2927T>A
MANE Select
|
ENSP00000417980.1:p.Leu976Gln
|
|
ENST00000636027.1:c.2813T>A
|
ENSP00000489961.1:p.Leu938Gln
|
|
ENST00000637161.1:c.2834T>A
|
ENSP00000490328.1:p.Leu945Gln
|
|
ENST00000637261.1:c.2967T>A
|
ENSP00000490815.1:n.2967T>A
|
|
ENST00000637891.1:c.821T>A
|
ENSP00000490907.1:p.Leu274Gln
|
|
ENST00000460843.5:c.2927T>A
|
ENSP00000417980.1:p.Leu976Gln
|
|
ENST00000462942.3:c.1784T>A
|
ENSP00000436107.1:p.Leu595Gln
|
|
ENST00000486164.5:c.614T>A
|
|
|
ENST00000488242.2:n.453T>A
|
|
|
NM_024757.4:c.2927T>A
|
NP_079033.4:p.Leu976Gln
|
|
XM_005266105.3:c.2918T>A
|
XP_005266162.1:p.Leu973Gln
|
|
XM_005266110.1:c.2834T>A
|
XP_005266167.1:p.Leu945Gln
|
|
XM_006717288.2:c.2909T>A
|
XP_006717351.1:p.Leu970Gln
|
|
XM_011519021.1:c.2936T>A
|
XP_011517323.1:p.Leu979Gln
|
|
XM_011519022.1:c.2933T>A
|
XP_011517324.1:p.Leu978Gln
|
|
XM_011519023.1:c.2915T>A
|
XP_011517325.1:p.Leu972Gln
|
|
XM_011519024.1:c.2858T>A
|
XP_011517326.1:p.Leu953Gln
|
|
XM_011519025.1:c.2834T>A
|
XP_011517327.1:p.Leu945Gln
|
|
XM_011519026.1:c.2792T>A
|
XP_011517328.1:p.Leu931Gln
|
|
XM_011519029.1:c.1358T>A
|
XP_011517331.1:p.Leu453Gln
|
|
XM_011519030.1:c.710T>A
|
XP_011517332.1:p.Leu237Gln
|
|
XM_011519031.1:c.497T>A
|
XP_011517333.1:p.Leu166Gln
|
|
XM_011519032.1:c.497T>A
|
XP_011517334.1:p.Leu166Gln
|
|
XM_011519033.1:c.2771T>A
|
XP_011517335.1:p.Leu924Gln
|
|
NM_001354263.1:c.2906T>A
|
NP_001341192.1:p.Leu969Gln
|
|
XM_005266105.5:c.2918T>A
|
XP_005266162.1:p.Leu973Gln
|
|
XM_011519021.3:c.2936T>A
|
XP_011517323.1:p.Leu979Gln
|
|
XM_011519022.3:c.2933T>A
|
XP_011517324.1:p.Leu978Gln
|
|
XM_011519023.3:c.2915T>A
|
XP_011517325.1:p.Leu972Gln
|
|
XM_011519029.3:c.1358T>A
|
XP_011517331.1:p.Leu453Gln
|
|
XM_011519030.3:c.710T>A
|
XP_011517332.1:p.Leu237Gln
|
|
XM_017015134.1:c.2912T>A
|
XP_016870623.1:p.Leu971Gln
|
|
XM_017015136.2:c.2828T>A
|
XP_016870625.1:p.Leu943Gln
|
|
XM_017015137.1:c.2813T>A
|
XP_016870626.1:p.Leu938Gln
|
|
XM_017015138.1:c.2813T>A
|
XP_016870627.1:p.Leu938Gln
|
|
XM_024447674.1:c.2756T>A
|
XP_024303442.1:p.Leu919Gln
|
|
XM_024447675.1:c.2690T>A
|
XP_024303443.1:p.Leu897Gln
|
|
XM_024447676.1:c.2051T>A
|
XP_024303444.1:p.Leu684Gln
|
|
XM_024447677.1:c.2051T>A
|
XP_024303445.1:p.Leu684Gln
|
|
XM_024447680.1:c.2669T>A
|
XP_024303448.1:p.Leu890Gln
|
|
NM_024757.5:c.2927T>A
MANE Select
|
NP_079033.4:p.Leu976Gln
|
|
NM_001354263.2:c.2906T>A
|
NP_001341192.1:p.Leu969Gln
|
|