ENST00000460843.6:c.2679G>T
MANE Select
|
ENSP00000417980.1:p.Leu893=
|
|
ENST00000636027.1:c.2565G>T
|
ENSP00000489961.1:p.Leu855=
|
|
ENST00000637161.1:c.2586G>T
|
ENSP00000490328.1:p.Leu862=
|
|
ENST00000637261.1:c.2719G>T
|
ENSP00000490815.1:n.2719G>T
|
|
ENST00000637891.1:c.573G>T
|
ENSP00000490907.1:p.Leu191=
|
|
ENST00000637949.1:c.357G>T
|
ENSP00000489786.1:p.Leu119=
|
|
ENST00000460843.5:c.2679G>T
|
ENSP00000417980.1:p.Leu893=
|
|
ENST00000462942.3:c.1536G>T
|
ENSP00000436107.1:p.Leu512=
|
|
ENST00000482340.5:c.249G>T
|
ENSP00000486748.1:p.Leu83=
|
|
ENST00000486164.5:c.257G>T
|
|
|
ENST00000488242.2:n.205G>T
|
|
|
ENST00000493484.5:c.249G>T
|
ENSP00000486503.1:p.Leu83=
|
|
NM_024757.4:c.2679G>T
|
NP_079033.4:p.Leu893=
|
|
XM_005266105.3:c.2670G>T
|
XP_005266162.1:p.Leu890=
|
|
XM_005266110.1:c.2586G>T
|
XP_005266167.1:p.Leu862=
|
|
XM_006717288.2:c.2661G>T
|
XP_006717351.1:p.Leu887=
|
|
XM_011519021.1:c.2688G>T
|
XP_011517323.1:p.Leu896=
|
|
XM_011519022.1:c.2685G>T
|
XP_011517324.1:p.Leu895=
|
|
XM_011519023.1:c.2667G>T
|
XP_011517325.1:p.Leu889=
|
|
XM_011519024.1:c.2610G>T
|
XP_011517326.1:p.Leu870=
|
|
XM_011519025.1:c.2586G>T
|
XP_011517327.1:p.Leu862=
|
|
XM_011519026.1:c.2544G>T
|
XP_011517328.1:p.Leu848=
|
|
XM_011519027.1:c.2688G>T
|
XP_011517329.1:p.Leu896=
|
|
XM_011519029.1:c.1110G>T
|
XP_011517331.1:p.Leu370=
|
|
XM_011519030.1:c.462G>T
|
XP_011517332.1:p.Leu154=
|
|
XM_011519031.1:c.249G>T
|
XP_011517333.1:p.Leu83=
|
|
XM_011519032.1:c.249G>T
|
XP_011517334.1:p.Leu83=
|
|
XM_011519033.1:c.2523G>T
|
XP_011517335.1:p.Leu841=
|
|
NM_001354263.1:c.2658G>T
|
NP_001341192.1:p.Leu886=
|
|
XM_005266105.5:c.2670G>T
|
XP_005266162.1:p.Leu890=
|
|
XM_011519021.3:c.2688G>T
|
XP_011517323.1:p.Leu896=
|
|
XM_011519022.3:c.2685G>T
|
XP_011517324.1:p.Leu895=
|
|
XM_011519023.3:c.2667G>T
|
XP_011517325.1:p.Leu889=
|
|
XM_011519029.3:c.1110G>T
|
XP_011517331.1:p.Leu370=
|
|
XM_011519030.3:c.462G>T
|
XP_011517332.1:p.Leu154=
|
|
XM_017015134.1:c.2664G>T
|
XP_016870623.1:p.Leu888=
|
|
XM_017015136.2:c.2580G>T
|
XP_016870625.1:p.Leu860=
|
|
XM_017015137.1:c.2565G>T
|
XP_016870626.1:p.Leu855=
|
|
XM_017015138.1:c.2565G>T
|
XP_016870627.1:p.Leu855=
|
|
XM_024447674.1:c.2508G>T
|
XP_024303442.1:p.Leu836=
|
|
XM_024447675.1:c.2442G>T
|
XP_024303443.1:p.Leu814=
|
|
XM_024447676.1:c.1803G>T
|
XP_024303444.1:p.Leu601=
|
|
XM_024447677.1:c.1803G>T
|
XP_024303445.1:p.Leu601=
|
|
XM_024447678.1:c.2586G>T
|
XP_024303446.1:p.Leu862=
|
|
XM_024447680.1:c.2421G>T
|
XP_024303448.1:p.Leu807=
|
|
NM_024757.5:c.2679G>T
MANE Select
|
NP_079033.4:p.Leu893=
|
|
NM_001354263.2:c.2658G>T
|
NP_001341192.1:p.Leu886=
|
|