ENST00000460843.6:c.2986C>T
MANE Select
|
ENSP00000417980.1:p.Gln996Ter
|
|
ENST00000636027.1:c.2872C>T
|
ENSP00000489961.1:p.Gln958Ter
|
|
ENST00000637161.1:c.2893C>T
|
ENSP00000490328.1:p.Gln965Ter
|
|
ENST00000637261.1:c.3026C>T
|
ENSP00000490815.1:n.3026C>T
|
|
ENST00000637891.1:c.880C>T
|
ENSP00000490907.1:p.Gln294Ter
|
|
ENST00000460843.5:c.2986C>T
|
ENSP00000417980.1:p.Gln996Ter
|
|
ENST00000462942.3:c.1843C>T
|
ENSP00000436107.1:p.Gln615Ter
|
|
ENST00000486164.5:c.673C>T
|
|
|
ENST00000488242.2:n.512C>T
|
|
|
NM_024757.4:c.2986C>T
|
NP_079033.4:p.Gln996Ter
|
|
XM_005266105.3:c.2977C>T
|
XP_005266162.1:p.Gln993Ter
|
|
XM_005266110.1:c.2893C>T
|
XP_005266167.1:p.Gln965Ter
|
|
XM_006717288.2:c.2968C>T
|
XP_006717351.1:p.Gln990Ter
|
|
XM_011519021.1:c.2995C>T
|
XP_011517323.1:p.Gln999Ter
|
|
XM_011519022.1:c.2992C>T
|
XP_011517324.1:p.Gln998Ter
|
|
XM_011519023.1:c.2974C>T
|
XP_011517325.1:p.Gln992Ter
|
|
XM_011519024.1:c.2917C>T
|
XP_011517326.1:p.Gln973Ter
|
|
XM_011519025.1:c.2893C>T
|
XP_011517327.1:p.Gln965Ter
|
|
XM_011519026.1:c.2851C>T
|
XP_011517328.1:p.Gln951Ter
|
|
XM_011519029.1:c.1417C>T
|
XP_011517331.1:p.Gln473Ter
|
|
XM_011519030.1:c.769C>T
|
XP_011517332.1:p.Gln257Ter
|
|
XM_011519031.1:c.556C>T
|
XP_011517333.1:p.Gln186Ter
|
|
XM_011519032.1:c.556C>T
|
XP_011517334.1:p.Gln186Ter
|
|
XM_011519033.1:c.2830C>T
|
XP_011517335.1:p.Gln944Ter
|
|
NM_001354263.1:c.2965C>T
|
NP_001341192.1:p.Gln989Ter
|
|
XM_005266105.5:c.2977C>T
|
XP_005266162.1:p.Gln993Ter
|
|
XM_011519021.3:c.2995C>T
|
XP_011517323.1:p.Gln999Ter
|
|
XM_011519022.3:c.2992C>T
|
XP_011517324.1:p.Gln998Ter
|
|
XM_011519023.3:c.2974C>T
|
XP_011517325.1:p.Gln992Ter
|
|
XM_011519029.3:c.1417C>T
|
XP_011517331.1:p.Gln473Ter
|
|
XM_011519030.3:c.769C>T
|
XP_011517332.1:p.Gln257Ter
|
|
XM_017015134.1:c.2971C>T
|
XP_016870623.1:p.Gln991Ter
|
|
XM_017015136.2:c.2887C>T
|
XP_016870625.1:p.Gln963Ter
|
|
XM_017015137.1:c.2872C>T
|
XP_016870626.1:p.Gln958Ter
|
|
XM_017015138.1:c.2872C>T
|
XP_016870627.1:p.Gln958Ter
|
|
XM_024447674.1:c.2815C>T
|
XP_024303442.1:p.Gln939Ter
|
|
XM_024447675.1:c.2749C>T
|
XP_024303443.1:p.Gln917Ter
|
|
XM_024447676.1:c.2110C>T
|
XP_024303444.1:p.Gln704Ter
|
|
XM_024447677.1:c.2110C>T
|
XP_024303445.1:p.Gln704Ter
|
|
XM_024447680.1:c.2728C>T
|
XP_024303448.1:p.Gln910Ter
|
|
NM_024757.5:c.2986C>T
MANE Select
|
NP_079033.4:p.Gln996Ter
|
|
NM_001354263.2:c.2965C>T
|
NP_001341192.1:p.Gln989Ter
|
|