ENST00000460843.6:c.3078C>T
MANE Select
|
ENSP00000417980.1:p.Val1026=
|
|
ENST00000637161.1:c.2985C>T
|
ENSP00000490328.1:p.Val995=
|
|
ENST00000637261.1:c.3118C>T
|
ENSP00000490815.1:n.3118C>T
|
|
ENST00000637891.1:c.972C>T
|
ENSP00000490907.1:p.Val324=
|
|
ENST00000460843.5:c.3078C>T
|
ENSP00000417980.1:p.Val1026=
|
|
ENST00000462942.3:c.1935C>T
|
ENSP00000436107.1:p.Val645=
|
|
ENST00000486164.5:c.765C>T
|
|
|
ENST00000488242.2:n.604C>T
|
|
|
NM_024757.4:c.3078C>T
|
NP_079033.4:p.Val1026=
|
|
XM_005266105.3:c.3069C>T
|
XP_005266162.1:p.Val1023=
|
|
XM_005266110.1:c.2985C>T
|
XP_005266167.1:p.Val995=
|
|
XM_006717288.2:c.3060C>T
|
XP_006717351.1:p.Val1020=
|
|
XM_011519021.1:c.3087C>T
|
XP_011517323.1:p.Val1029=
|
|
XM_011519022.1:c.3084C>T
|
XP_011517324.1:p.Val1028=
|
|
XM_011519023.1:c.3066C>T
|
XP_011517325.1:p.Val1022=
|
|
XM_011519024.1:c.3009C>T
|
XP_011517326.1:p.Val1003=
|
|
XM_011519025.1:c.2985C>T
|
XP_011517327.1:p.Val995=
|
|
XM_011519026.1:c.2943C>T
|
XP_011517328.1:p.Val981=
|
|
XM_011519029.1:c.1509C>T
|
XP_011517331.1:p.Val503=
|
|
XM_011519030.1:c.861C>T
|
XP_011517332.1:p.Val287=
|
|
XM_011519031.1:c.648C>T
|
XP_011517333.1:p.Val216=
|
|
XM_011519032.1:c.648C>T
|
XP_011517334.1:p.Val216=
|
|
XM_011519033.1:c.2922C>T
|
XP_011517335.1:p.Val974=
|
|
NM_001354263.1:c.3057C>T
|
NP_001341192.1:p.Val1019=
|
|
XM_005266105.5:c.3069C>T
|
XP_005266162.1:p.Val1023=
|
|
XM_011519021.3:c.3087C>T
|
XP_011517323.1:p.Val1029=
|
|
XM_011519022.3:c.3084C>T
|
XP_011517324.1:p.Val1028=
|
|
XM_011519023.3:c.3066C>T
|
XP_011517325.1:p.Val1022=
|
|
XM_011519029.3:c.1509C>T
|
XP_011517331.1:p.Val503=
|
|
XM_011519030.3:c.861C>T
|
XP_011517332.1:p.Val287=
|
|
XM_017015134.1:c.3063C>T
|
XP_016870623.1:p.Val1021=
|
|
XM_017015136.2:c.2979C>T
|
XP_016870625.1:p.Val993=
|
|
XM_017015137.1:c.2964C>T
|
XP_016870626.1:p.Val988=
|
|
XM_017015138.1:c.2964C>T
|
XP_016870627.1:p.Val988=
|
|
XM_024447674.1:c.2907C>T
|
XP_024303442.1:p.Val969=
|
|
XM_024447675.1:c.2841C>T
|
XP_024303443.1:p.Val947=
|
|
XM_024447676.1:c.2202C>T
|
XP_024303444.1:p.Val734=
|
|
XM_024447677.1:c.2202C>T
|
XP_024303445.1:p.Val734=
|
|
XM_024447680.1:c.2820C>T
|
XP_024303448.1:p.Val940=
|
|
NM_024757.5:c.3078C>T
MANE Select
|
NP_079033.4:p.Val1026=
|
|
NM_001354263.2:c.3057C>T
|
NP_001341192.1:p.Val1019=
|
|