ENST00000350026.11:c.3958A>T
|
ENSP00000055163.8:p.Lys1320Ter
|
|
ENST00000414678.8:c.4027A>T
|
ENSP00000412835.3:p.Lys1343Ter
|
|
ENST00000637015.2:c.4246A>T
|
ENSP00000489729.2:p.Lys1416Ter
|
|
ENST00000346085.10:c.3997A>T
|
ENSP00000344546.5:p.Lys1333Ter
|
|
ENST00000350026.10:c.3709A>T
|
ENSP00000055163.7:p.Lys1237Ter
|
|
ENST00000414678.7:c.2275A>T
|
ENSP00000412835.2:p.Lys759Ter
|
|
ENST00000635849.1:c.1438A>T
|
ENSP00000490948.1:p.Lys480Ter
|
|
ENST00000635957.1:c.1069A>T
|
ENSP00000490385.1:p.Lys357Ter
|
|
ENST00000636930.2:c.4117A>T
MANE Select
|
ENSP00000490491.2:p.Lys1373Ter
|
|
ENST00000636940.1:n.2114A>T
|
|
|
ENST00000637015.1:c.1485A>T
|
|
|
ENST00000637568.1:c.1399A>T
|
|
|
ENST00000637741.1:n.783A>T
|
|
|
ENST00000637810.1:c.1459A>T
|
ENSP00000489636.1:p.Lys487Ter
|
|
ENST00000637904.1:c.1618A>T
|
ENSP00000490550.1:p.Lys540Ter
|
|
ENST00000647938.1:c.3748A>T
|
ENSP00000498155.1:p.Lys1250Ter
|
|
ENST00000346085.9:c.3748A>T
|
ENSP00000344546.4:p.Lys1250Ter
|
|
ENST00000350026.9:c.3709A>T
|
ENSP00000055163.7:p.Lys1237Ter
|
|
ENST00000414678.6:c.2275A>T
|
ENSP00000412835.2:p.Lys759Ter
|
|
NM_017519.2:c.3709A>T
|
NP_059989.2:p.Lys1237Ter
|
|
NM_020732.3:c.3748A>T
|
NP_065783.3:p.Lys1250Ter
|
|
XM_005267069.3:c.3868A>T
|
XP_005267126.2:p.Lys1290Ter
|
|
XM_011535984.1:c.2947A>T
|
XP_011534286.1:p.Lys983Ter
|
|
XM_011535985.1:c.2767A>T
|
XP_011534287.1:p.Lys923Ter
|
|
XM_011535986.1:c.2527A>T
|
XP_011534288.1:p.Lys843Ter
|
|
XM_011535987.1:c.2146A>T
|
XP_011534289.1:p.Lys716Ter
|
|
XM_011535988.1:c.1009A>T
|
XP_011534290.1:p.Lys337Ter
|
|
NM_001346813.1:c.3868A>T
|
NP_001333742.1:p.Lys1290Ter
|
|
NM_001363725.1:c.1618A>T
|
NP_001350654.1:p.Lys540Ter
|
|
XM_011535984.2:c.4078A>T
|
XP_011534286.2:p.Lys1360Ter
|
|
XM_011535988.3:c.1009A>T
|
XP_011534290.1:p.Lys337Ter
|
|
XM_017011103.2:c.3979A>T
|
XP_016866592.1:p.Lys1327Ter
|
|
XM_017011104.1:c.3949A>T
|
XP_016866593.1:p.Lys1317Ter
|
|
XM_017011105.2:c.3919A>T
|
XP_016866594.1:p.Lys1307Ter
|
|
XM_017011106.2:c.3790A>T
|
XP_016866595.1:p.Lys1264Ter
|
|
XM_017011107.2:c.3769A>T
|
XP_016866596.1:p.Lys1257Ter
|
|
XR_002956289.1:n.4161A>T
|
|
|
NM_001363725.2:c.1618A>T
|
NP_001350654.1:p.Lys540Ter
|
|
NM_001371656.1:c.3997A>T
|
NP_001358585.1:p.Lys1333Ter
|
|
NM_001374820.1:c.3997A>T
|
NP_001361749.1:p.Lys1333Ter
|
|
NM_001374828.1:c.4117A>T
MANE Select
|
NP_001361757.1:p.Lys1373Ter
|
|
NM_017519.3:c.3958A>T
|
NP_059989.3:p.Lys1320Ter
|
|