ENST00000460843.6:c.2903A>T
MANE Select
|
ENSP00000417980.1:p.Lys968Met
|
|
ENST00000636027.1:c.2789A>T
|
ENSP00000489961.1:p.Lys930Met
|
|
ENST00000637161.1:c.2810A>T
|
ENSP00000490328.1:p.Lys937Met
|
|
ENST00000637261.1:c.2943A>T
|
ENSP00000490815.1:n.2943A>T
|
|
ENST00000637891.1:c.797A>T
|
ENSP00000490907.1:p.Lys266Met
|
|
ENST00000460843.5:c.2903A>T
|
ENSP00000417980.1:p.Lys968Met
|
|
ENST00000462942.3:c.1760A>T
|
ENSP00000436107.1:p.Lys587Met
|
|
ENST00000486164.5:c.590A>T
|
|
|
ENST00000488242.2:n.429A>T
|
|
|
NM_024757.4:c.2903A>T
|
NP_079033.4:p.Lys968Met
|
|
XM_005266105.3:c.2894A>T
|
XP_005266162.1:p.Lys965Met
|
|
XM_005266110.1:c.2810A>T
|
XP_005266167.1:p.Lys937Met
|
|
XM_006717288.2:c.2885A>T
|
XP_006717351.1:p.Lys962Met
|
|
XM_011519021.1:c.2912A>T
|
XP_011517323.1:p.Lys971Met
|
|
XM_011519022.1:c.2909A>T
|
XP_011517324.1:p.Lys970Met
|
|
XM_011519023.1:c.2891A>T
|
XP_011517325.1:p.Lys964Met
|
|
XM_011519024.1:c.2834A>T
|
XP_011517326.1:p.Lys945Met
|
|
XM_011519025.1:c.2810A>T
|
XP_011517327.1:p.Lys937Met
|
|
XM_011519026.1:c.2768A>T
|
XP_011517328.1:p.Lys923Met
|
|
XM_011519029.1:c.1334A>T
|
XP_011517331.1:p.Lys445Met
|
|
XM_011519030.1:c.686A>T
|
XP_011517332.1:p.Lys229Met
|
|
XM_011519031.1:c.473A>T
|
XP_011517333.1:p.Lys158Met
|
|
XM_011519032.1:c.473A>T
|
XP_011517334.1:p.Lys158Met
|
|
XM_011519033.1:c.2747A>T
|
XP_011517335.1:p.Lys916Met
|
|
NM_001354263.1:c.2882A>T
|
NP_001341192.1:p.Lys961Met
|
|
XM_005266105.5:c.2894A>T
|
XP_005266162.1:p.Lys965Met
|
|
XM_011519021.3:c.2912A>T
|
XP_011517323.1:p.Lys971Met
|
|
XM_011519022.3:c.2909A>T
|
XP_011517324.1:p.Lys970Met
|
|
XM_011519023.3:c.2891A>T
|
XP_011517325.1:p.Lys964Met
|
|
XM_011519029.3:c.1334A>T
|
XP_011517331.1:p.Lys445Met
|
|
XM_011519030.3:c.686A>T
|
XP_011517332.1:p.Lys229Met
|
|
XM_017015134.1:c.2888A>T
|
XP_016870623.1:p.Lys963Met
|
|
XM_017015136.2:c.2804A>T
|
XP_016870625.1:p.Lys935Met
|
|
XM_017015137.1:c.2789A>T
|
XP_016870626.1:p.Lys930Met
|
|
XM_017015138.1:c.2789A>T
|
XP_016870627.1:p.Lys930Met
|
|
XM_024447674.1:c.2732A>T
|
XP_024303442.1:p.Lys911Met
|
|
XM_024447675.1:c.2666A>T
|
XP_024303443.1:p.Lys889Met
|
|
XM_024447676.1:c.2027A>T
|
XP_024303444.1:p.Lys676Met
|
|
XM_024447677.1:c.2027A>T
|
XP_024303445.1:p.Lys676Met
|
|
XM_024447680.1:c.2645A>T
|
XP_024303448.1:p.Lys882Met
|
|
NM_024757.5:c.2903A>T
MANE Select
|
NP_079033.4:p.Lys968Met
|
|
NM_001354263.2:c.2882A>T
|
NP_001341192.1:p.Lys961Met
|
|