ENST00000460843.6:c.2943C>A
MANE Select
|
ENSP00000417980.1:p.Leu981=
|
|
ENST00000636027.1:c.2829C>A
|
ENSP00000489961.1:p.Leu943=
|
|
ENST00000637161.1:c.2850C>A
|
ENSP00000490328.1:p.Leu950=
|
|
ENST00000637261.1:c.2983C>A
|
ENSP00000490815.1:n.2983C>A
|
|
ENST00000637891.1:c.837C>A
|
ENSP00000490907.1:p.Leu279=
|
|
ENST00000460843.5:c.2943C>A
|
ENSP00000417980.1:p.Leu981=
|
|
ENST00000462942.3:c.1800C>A
|
ENSP00000436107.1:p.Leu600=
|
|
ENST00000486164.5:c.630C>A
|
|
|
ENST00000488242.2:n.469C>A
|
|
|
NM_024757.4:c.2943C>A
|
NP_079033.4:p.Leu981=
|
|
XM_005266105.3:c.2934C>A
|
XP_005266162.1:p.Leu978=
|
|
XM_005266110.1:c.2850C>A
|
XP_005266167.1:p.Leu950=
|
|
XM_006717288.2:c.2925C>A
|
XP_006717351.1:p.Leu975=
|
|
XM_011519021.1:c.2952C>A
|
XP_011517323.1:p.Leu984=
|
|
XM_011519022.1:c.2949C>A
|
XP_011517324.1:p.Leu983=
|
|
XM_011519023.1:c.2931C>A
|
XP_011517325.1:p.Leu977=
|
|
XM_011519024.1:c.2874C>A
|
XP_011517326.1:p.Leu958=
|
|
XM_011519025.1:c.2850C>A
|
XP_011517327.1:p.Leu950=
|
|
XM_011519026.1:c.2808C>A
|
XP_011517328.1:p.Leu936=
|
|
XM_011519029.1:c.1374C>A
|
XP_011517331.1:p.Leu458=
|
|
XM_011519030.1:c.726C>A
|
XP_011517332.1:p.Leu242=
|
|
XM_011519031.1:c.513C>A
|
XP_011517333.1:p.Leu171=
|
|
XM_011519032.1:c.513C>A
|
XP_011517334.1:p.Leu171=
|
|
XM_011519033.1:c.2787C>A
|
XP_011517335.1:p.Leu929=
|
|
NM_001354263.1:c.2922C>A
|
NP_001341192.1:p.Leu974=
|
|
XM_005266105.5:c.2934C>A
|
XP_005266162.1:p.Leu978=
|
|
XM_011519021.3:c.2952C>A
|
XP_011517323.1:p.Leu984=
|
|
XM_011519022.3:c.2949C>A
|
XP_011517324.1:p.Leu983=
|
|
XM_011519023.3:c.2931C>A
|
XP_011517325.1:p.Leu977=
|
|
XM_011519029.3:c.1374C>A
|
XP_011517331.1:p.Leu458=
|
|
XM_011519030.3:c.726C>A
|
XP_011517332.1:p.Leu242=
|
|
XM_017015134.1:c.2928C>A
|
XP_016870623.1:p.Leu976=
|
|
XM_017015136.2:c.2844C>A
|
XP_016870625.1:p.Leu948=
|
|
XM_017015137.1:c.2829C>A
|
XP_016870626.1:p.Leu943=
|
|
XM_017015138.1:c.2829C>A
|
XP_016870627.1:p.Leu943=
|
|
XM_024447674.1:c.2772C>A
|
XP_024303442.1:p.Leu924=
|
|
XM_024447675.1:c.2706C>A
|
XP_024303443.1:p.Leu902=
|
|
XM_024447676.1:c.2067C>A
|
XP_024303444.1:p.Leu689=
|
|
XM_024447677.1:c.2067C>A
|
XP_024303445.1:p.Leu689=
|
|
XM_024447680.1:c.2685C>A
|
XP_024303448.1:p.Leu895=
|
|
NM_024757.5:c.2943C>A
MANE Select
|
NP_079033.4:p.Leu981=
|
|
NM_001354263.2:c.2922C>A
|
NP_001341192.1:p.Leu974=
|
|