|
ENST00000460843.6:c.2674C>G
MANE Select
|
ENSP00000417980.1:p.Leu892Val
|
|
|
ENST00000636027.1:c.2560C>G
|
ENSP00000489961.1:p.Leu854Val
|
|
|
ENST00000637161.1:c.2581C>G
|
ENSP00000490328.1:p.Leu861Val
|
|
|
ENST00000637261.1:c.2714C>G
|
ENSP00000490815.1:n.2714C>G
|
|
|
ENST00000637891.1:c.568C>G
|
ENSP00000490907.1:p.Leu190Val
|
|
|
ENST00000637949.1:c.352C>G
|
ENSP00000489786.1:p.Leu118Val
|
|
|
ENST00000460843.5:c.2674C>G
|
ENSP00000417980.1:p.Leu892Val
|
|
|
ENST00000462942.3:c.1531C>G
|
ENSP00000436107.1:p.Leu511Val
|
|
|
ENST00000482340.5:c.244C>G
|
ENSP00000486748.1:p.Leu82Val
|
|
|
ENST00000486164.5:c.252C>G
|
|
|
|
ENST00000488242.2:n.200C>G
|
|
|
|
ENST00000493484.5:c.244C>G
|
ENSP00000486503.1:p.Leu82Val
|
|
|
NM_024757.4:c.2674C>G
|
NP_079033.4:p.Leu892Val
|
|
|
XM_005266105.3:c.2665C>G
|
XP_005266162.1:p.Leu889Val
|
|
|
XM_005266110.1:c.2581C>G
|
XP_005266167.1:p.Leu861Val
|
|
|
XM_006717288.2:c.2656C>G
|
XP_006717351.1:p.Leu886Val
|
|
|
XM_011519021.1:c.2683C>G
|
XP_011517323.1:p.Leu895Val
|
|
|
XM_011519022.1:c.2680C>G
|
XP_011517324.1:p.Leu894Val
|
|
|
XM_011519023.1:c.2662C>G
|
XP_011517325.1:p.Leu888Val
|
|
|
XM_011519024.1:c.2605C>G
|
XP_011517326.1:p.Leu869Val
|
|
|
XM_011519025.1:c.2581C>G
|
XP_011517327.1:p.Leu861Val
|
|
|
XM_011519026.1:c.2539C>G
|
XP_011517328.1:p.Leu847Val
|
|
|
XM_011519027.1:c.2683C>G
|
XP_011517329.1:p.Leu895Val
|
|
|
XM_011519029.1:c.1105C>G
|
XP_011517331.1:p.Leu369Val
|
|
|
XM_011519030.1:c.457C>G
|
XP_011517332.1:p.Leu153Val
|
|
|
XM_011519031.1:c.244C>G
|
XP_011517333.1:p.Leu82Val
|
|
|
XM_011519032.1:c.244C>G
|
XP_011517334.1:p.Leu82Val
|
|
|
XM_011519033.1:c.2518C>G
|
XP_011517335.1:p.Leu840Val
|
|
|
NM_001354263.1:c.2653C>G
|
NP_001341192.1:p.Leu885Val
|
|
|
XM_005266105.5:c.2665C>G
|
XP_005266162.1:p.Leu889Val
|
|
|
XM_011519021.3:c.2683C>G
|
XP_011517323.1:p.Leu895Val
|
|
|
XM_011519022.3:c.2680C>G
|
XP_011517324.1:p.Leu894Val
|
|
|
XM_011519023.3:c.2662C>G
|
XP_011517325.1:p.Leu888Val
|
|
|
XM_011519029.3:c.1105C>G
|
XP_011517331.1:p.Leu369Val
|
|
|
XM_011519030.3:c.457C>G
|
XP_011517332.1:p.Leu153Val
|
|
|
XM_017015134.1:c.2659C>G
|
XP_016870623.1:p.Leu887Val
|
|
|
XM_017015136.2:c.2575C>G
|
XP_016870625.1:p.Leu859Val
|
|
|
XM_017015137.1:c.2560C>G
|
XP_016870626.1:p.Leu854Val
|
|
|
XM_017015138.1:c.2560C>G
|
XP_016870627.1:p.Leu854Val
|
|
|
XM_024447674.1:c.2503C>G
|
XP_024303442.1:p.Leu835Val
|
|
|
XM_024447675.1:c.2437C>G
|
XP_024303443.1:p.Leu813Val
|
|
|
XM_024447676.1:c.1798C>G
|
XP_024303444.1:p.Leu600Val
|
|
|
XM_024447677.1:c.1798C>G
|
XP_024303445.1:p.Leu600Val
|
|
|
XM_024447678.1:c.2581C>G
|
XP_024303446.1:p.Leu861Val
|
|
|
XM_024447680.1:c.2416C>G
|
XP_024303448.1:p.Leu806Val
|
|
|
NM_024757.5:c.2674C>G
MANE Select
|
NP_079033.4:p.Leu892Val
|
|
|
NM_001354263.2:c.2653C>G
|
NP_001341192.1:p.Leu885Val
|
|
