ENST00000460843.6:c.2941C>G
MANE Select
|
ENSP00000417980.1:p.Leu981Val
|
|
ENST00000636027.1:c.2827C>G
|
ENSP00000489961.1:p.Leu943Val
|
|
ENST00000637161.1:c.2848C>G
|
ENSP00000490328.1:p.Leu950Val
|
|
ENST00000637261.1:c.2981C>G
|
ENSP00000490815.1:n.2981C>G
|
|
ENST00000637891.1:c.835C>G
|
ENSP00000490907.1:p.Leu279Val
|
|
ENST00000460843.5:c.2941C>G
|
ENSP00000417980.1:p.Leu981Val
|
|
ENST00000462942.3:c.1798C>G
|
ENSP00000436107.1:p.Leu600Val
|
|
ENST00000486164.5:c.628C>G
|
|
|
ENST00000488242.2:n.467C>G
|
|
|
NM_024757.4:c.2941C>G
|
NP_079033.4:p.Leu981Val
|
|
XM_005266105.3:c.2932C>G
|
XP_005266162.1:p.Leu978Val
|
|
XM_005266110.1:c.2848C>G
|
XP_005266167.1:p.Leu950Val
|
|
XM_006717288.2:c.2923C>G
|
XP_006717351.1:p.Leu975Val
|
|
XM_011519021.1:c.2950C>G
|
XP_011517323.1:p.Leu984Val
|
|
XM_011519022.1:c.2947C>G
|
XP_011517324.1:p.Leu983Val
|
|
XM_011519023.1:c.2929C>G
|
XP_011517325.1:p.Leu977Val
|
|
XM_011519024.1:c.2872C>G
|
XP_011517326.1:p.Leu958Val
|
|
XM_011519025.1:c.2848C>G
|
XP_011517327.1:p.Leu950Val
|
|
XM_011519026.1:c.2806C>G
|
XP_011517328.1:p.Leu936Val
|
|
XM_011519029.1:c.1372C>G
|
XP_011517331.1:p.Leu458Val
|
|
XM_011519030.1:c.724C>G
|
XP_011517332.1:p.Leu242Val
|
|
XM_011519031.1:c.511C>G
|
XP_011517333.1:p.Leu171Val
|
|
XM_011519032.1:c.511C>G
|
XP_011517334.1:p.Leu171Val
|
|
XM_011519033.1:c.2785C>G
|
XP_011517335.1:p.Leu929Val
|
|
NM_001354263.1:c.2920C>G
|
NP_001341192.1:p.Leu974Val
|
|
XM_005266105.5:c.2932C>G
|
XP_005266162.1:p.Leu978Val
|
|
XM_011519021.3:c.2950C>G
|
XP_011517323.1:p.Leu984Val
|
|
XM_011519022.3:c.2947C>G
|
XP_011517324.1:p.Leu983Val
|
|
XM_011519023.3:c.2929C>G
|
XP_011517325.1:p.Leu977Val
|
|
XM_011519029.3:c.1372C>G
|
XP_011517331.1:p.Leu458Val
|
|
XM_011519030.3:c.724C>G
|
XP_011517332.1:p.Leu242Val
|
|
XM_017015134.1:c.2926C>G
|
XP_016870623.1:p.Leu976Val
|
|
XM_017015136.2:c.2842C>G
|
XP_016870625.1:p.Leu948Val
|
|
XM_017015137.1:c.2827C>G
|
XP_016870626.1:p.Leu943Val
|
|
XM_017015138.1:c.2827C>G
|
XP_016870627.1:p.Leu943Val
|
|
XM_024447674.1:c.2770C>G
|
XP_024303442.1:p.Leu924Val
|
|
XM_024447675.1:c.2704C>G
|
XP_024303443.1:p.Leu902Val
|
|
XM_024447676.1:c.2065C>G
|
XP_024303444.1:p.Leu689Val
|
|
XM_024447677.1:c.2065C>G
|
XP_024303445.1:p.Leu689Val
|
|
XM_024447680.1:c.2683C>G
|
XP_024303448.1:p.Leu895Val
|
|
NM_024757.5:c.2941C>G
MANE Select
|
NP_079033.4:p.Leu981Val
|
|
NM_001354263.2:c.2920C>G
|
NP_001341192.1:p.Leu974Val
|
|