ENST00000460843.6:c.2893G>T
MANE Select
|
ENSP00000417980.1:p.Val965Phe
|
|
ENST00000636027.1:c.2779G>T
|
ENSP00000489961.1:p.Val927Phe
|
|
ENST00000637161.1:c.2800G>T
|
ENSP00000490328.1:p.Val934Phe
|
|
ENST00000637261.1:c.2933G>T
|
ENSP00000490815.1:n.2933G>T
|
|
ENST00000637891.1:c.787G>T
|
ENSP00000490907.1:p.Val263Phe
|
|
ENST00000460843.5:c.2893G>T
|
ENSP00000417980.1:p.Val965Phe
|
|
ENST00000462942.3:c.1750G>T
|
ENSP00000436107.1:p.Val584Phe
|
|
ENST00000486164.5:c.580G>T
|
|
|
ENST00000488242.2:n.419G>T
|
|
|
NM_024757.4:c.2893G>T
|
NP_079033.4:p.Val965Phe
|
|
XM_005266105.3:c.2884G>T
|
XP_005266162.1:p.Val962Phe
|
|
XM_005266110.1:c.2800G>T
|
XP_005266167.1:p.Val934Phe
|
|
XM_006717288.2:c.2875G>T
|
XP_006717351.1:p.Val959Phe
|
|
XM_011519021.1:c.2902G>T
|
XP_011517323.1:p.Val968Phe
|
|
XM_011519022.1:c.2899G>T
|
XP_011517324.1:p.Val967Phe
|
|
XM_011519023.1:c.2881G>T
|
XP_011517325.1:p.Val961Phe
|
|
XM_011519024.1:c.2824G>T
|
XP_011517326.1:p.Val942Phe
|
|
XM_011519025.1:c.2800G>T
|
XP_011517327.1:p.Val934Phe
|
|
XM_011519026.1:c.2758G>T
|
XP_011517328.1:p.Val920Phe
|
|
XM_011519029.1:c.1324G>T
|
XP_011517331.1:p.Val442Phe
|
|
XM_011519030.1:c.676G>T
|
XP_011517332.1:p.Val226Phe
|
|
XM_011519031.1:c.463G>T
|
XP_011517333.1:p.Val155Phe
|
|
XM_011519032.1:c.463G>T
|
XP_011517334.1:p.Val155Phe
|
|
XM_011519033.1:c.2737G>T
|
XP_011517335.1:p.Val913Phe
|
|
NM_001354263.1:c.2872G>T
|
NP_001341192.1:p.Val958Phe
|
|
XM_005266105.5:c.2884G>T
|
XP_005266162.1:p.Val962Phe
|
|
XM_011519021.3:c.2902G>T
|
XP_011517323.1:p.Val968Phe
|
|
XM_011519022.3:c.2899G>T
|
XP_011517324.1:p.Val967Phe
|
|
XM_011519023.3:c.2881G>T
|
XP_011517325.1:p.Val961Phe
|
|
XM_011519029.3:c.1324G>T
|
XP_011517331.1:p.Val442Phe
|
|
XM_011519030.3:c.676G>T
|
XP_011517332.1:p.Val226Phe
|
|
XM_017015134.1:c.2878G>T
|
XP_016870623.1:p.Val960Phe
|
|
XM_017015136.2:c.2794G>T
|
XP_016870625.1:p.Val932Phe
|
|
XM_017015137.1:c.2779G>T
|
XP_016870626.1:p.Val927Phe
|
|
XM_017015138.1:c.2779G>T
|
XP_016870627.1:p.Val927Phe
|
|
XM_024447674.1:c.2722G>T
|
XP_024303442.1:p.Val908Phe
|
|
XM_024447675.1:c.2656G>T
|
XP_024303443.1:p.Val886Phe
|
|
XM_024447676.1:c.2017G>T
|
XP_024303444.1:p.Val673Phe
|
|
XM_024447677.1:c.2017G>T
|
XP_024303445.1:p.Val673Phe
|
|
XM_024447680.1:c.2635G>T
|
XP_024303448.1:p.Val879Phe
|
|
NM_024757.5:c.2893G>T
MANE Select
|
NP_079033.4:p.Val965Phe
|
|
NM_001354263.2:c.2872G>T
|
NP_001341192.1:p.Val958Phe
|
|