ENST00000460843.6:c.2899T>C
MANE Select
|
ENSP00000417980.1:p.Leu967=
|
|
ENST00000636027.1:c.2785T>C
|
ENSP00000489961.1:p.Leu929=
|
|
ENST00000637161.1:c.2806T>C
|
ENSP00000490328.1:p.Leu936=
|
|
ENST00000637261.1:c.2939T>C
|
ENSP00000490815.1:n.2939T>C
|
|
ENST00000637891.1:c.793T>C
|
ENSP00000490907.1:p.Leu265=
|
|
ENST00000460843.5:c.2899T>C
|
ENSP00000417980.1:p.Leu967=
|
|
ENST00000462942.3:c.1756T>C
|
ENSP00000436107.1:p.Leu586=
|
|
ENST00000486164.5:c.586T>C
|
|
|
ENST00000488242.2:n.425T>C
|
|
|
NM_024757.4:c.2899T>C
|
NP_079033.4:p.Leu967=
|
|
XM_005266105.3:c.2890T>C
|
XP_005266162.1:p.Leu964=
|
|
XM_005266110.1:c.2806T>C
|
XP_005266167.1:p.Leu936=
|
|
XM_006717288.2:c.2881T>C
|
XP_006717351.1:p.Leu961=
|
|
XM_011519021.1:c.2908T>C
|
XP_011517323.1:p.Leu970=
|
|
XM_011519022.1:c.2905T>C
|
XP_011517324.1:p.Leu969=
|
|
XM_011519023.1:c.2887T>C
|
XP_011517325.1:p.Leu963=
|
|
XM_011519024.1:c.2830T>C
|
XP_011517326.1:p.Leu944=
|
|
XM_011519025.1:c.2806T>C
|
XP_011517327.1:p.Leu936=
|
|
XM_011519026.1:c.2764T>C
|
XP_011517328.1:p.Leu922=
|
|
XM_011519029.1:c.1330T>C
|
XP_011517331.1:p.Leu444=
|
|
XM_011519030.1:c.682T>C
|
XP_011517332.1:p.Leu228=
|
|
XM_011519031.1:c.469T>C
|
XP_011517333.1:p.Leu157=
|
|
XM_011519032.1:c.469T>C
|
XP_011517334.1:p.Leu157=
|
|
XM_011519033.1:c.2743T>C
|
XP_011517335.1:p.Leu915=
|
|
NM_001354263.1:c.2878T>C
|
NP_001341192.1:p.Leu960=
|
|
XM_005266105.5:c.2890T>C
|
XP_005266162.1:p.Leu964=
|
|
XM_011519021.3:c.2908T>C
|
XP_011517323.1:p.Leu970=
|
|
XM_011519022.3:c.2905T>C
|
XP_011517324.1:p.Leu969=
|
|
XM_011519023.3:c.2887T>C
|
XP_011517325.1:p.Leu963=
|
|
XM_011519029.3:c.1330T>C
|
XP_011517331.1:p.Leu444=
|
|
XM_011519030.3:c.682T>C
|
XP_011517332.1:p.Leu228=
|
|
XM_017015134.1:c.2884T>C
|
XP_016870623.1:p.Leu962=
|
|
XM_017015136.2:c.2800T>C
|
XP_016870625.1:p.Leu934=
|
|
XM_017015137.1:c.2785T>C
|
XP_016870626.1:p.Leu929=
|
|
XM_017015138.1:c.2785T>C
|
XP_016870627.1:p.Leu929=
|
|
XM_024447674.1:c.2728T>C
|
XP_024303442.1:p.Leu910=
|
|
XM_024447675.1:c.2662T>C
|
XP_024303443.1:p.Leu888=
|
|
XM_024447676.1:c.2023T>C
|
XP_024303444.1:p.Leu675=
|
|
XM_024447677.1:c.2023T>C
|
XP_024303445.1:p.Leu675=
|
|
XM_024447680.1:c.2641T>C
|
XP_024303448.1:p.Leu881=
|
|
NM_024757.5:c.2899T>C
MANE Select
|
NP_079033.4:p.Leu967=
|
|
NM_001354263.2:c.2878T>C
|
NP_001341192.1:p.Leu960=
|
|