ENST00000350026.11:c.3796C>A
|
ENSP00000055163.8:p.Gln1266Lys
|
|
ENST00000414678.8:c.3865C>A
|
ENSP00000412835.3:p.Gln1289Lys
|
|
ENST00000637015.2:c.4084C>A
|
ENSP00000489729.2:p.Gln1362Lys
|
|
ENST00000346085.10:c.3835C>A
|
ENSP00000344546.5:p.Gln1279Lys
|
|
ENST00000350026.10:c.3547C>A
|
ENSP00000055163.7:p.Gln1183Lys
|
|
ENST00000414678.7:c.2113C>A
|
ENSP00000412835.2:p.Gln705Lys
|
|
ENST00000635849.1:c.1276C>A
|
ENSP00000490948.1:p.Gln426Lys
|
|
ENST00000635957.1:c.910C>A
|
ENSP00000490385.1:p.Gln304Lys
|
|
ENST00000636930.2:c.3955C>A
MANE Select
|
ENSP00000490491.2:p.Gln1319Lys
|
|
ENST00000636940.1:n.1952C>A
|
|
|
ENST00000637015.1:c.1323C>A
|
|
|
ENST00000637568.1:c.1237C>A
|
|
|
ENST00000637741.1:n.621C>A
|
|
|
ENST00000637810.1:c.1297C>A
|
ENSP00000489636.1:p.Gln433Lys
|
|
ENST00000637904.1:c.1456C>A
|
ENSP00000490550.1:p.Gln486Lys
|
|
ENST00000647938.1:c.3586C>A
|
ENSP00000498155.1:p.Gln1196Lys
|
|
ENST00000346085.9:c.3586C>A
|
ENSP00000344546.4:p.Gln1196Lys
|
|
ENST00000350026.9:c.3547C>A
|
ENSP00000055163.7:p.Gln1183Lys
|
|
ENST00000414678.6:c.2113C>A
|
ENSP00000412835.2:p.Gln705Lys
|
|
NM_017519.2:c.3547C>A
|
NP_059989.2:p.Gln1183Lys
|
|
NM_020732.3:c.3586C>A
|
NP_065783.3:p.Gln1196Lys
|
|
XM_005267069.3:c.3706C>A
|
XP_005267126.2:p.Gln1236Lys
|
|
XM_011535984.1:c.2785C>A
|
XP_011534286.1:p.Gln929Lys
|
|
XM_011535985.1:c.2605C>A
|
XP_011534287.1:p.Gln869Lys
|
|
XM_011535986.1:c.2365C>A
|
XP_011534288.1:p.Gln789Lys
|
|
XM_011535987.1:c.1984C>A
|
XP_011534289.1:p.Gln662Lys
|
|
XM_011535988.1:c.847C>A
|
XP_011534290.1:p.Gln283Lys
|
|
NM_001346813.1:c.3706C>A
|
NP_001333742.1:p.Gln1236Lys
|
|
NM_001363725.1:c.1456C>A
|
NP_001350654.1:p.Gln486Lys
|
|
XM_011535984.2:c.3916C>A
|
XP_011534286.2:p.Gln1306Lys
|
|
XM_011535988.3:c.847C>A
|
XP_011534290.1:p.Gln283Lys
|
|
XM_017011103.2:c.3817C>A
|
XP_016866592.1:p.Gln1273Lys
|
|
XM_017011104.1:c.3787C>A
|
XP_016866593.1:p.Gln1263Lys
|
|
XM_017011105.2:c.3757C>A
|
XP_016866594.1:p.Gln1253Lys
|
|
XM_017011106.2:c.3628C>A
|
XP_016866595.1:p.Gln1210Lys
|
|
XM_017011107.2:c.3607C>A
|
XP_016866596.1:p.Gln1203Lys
|
|
XR_002956289.1:n.3999C>A
|
|
|
NM_001363725.2:c.1456C>A
|
NP_001350654.1:p.Gln486Lys
|
|
NM_001371656.1:c.3835C>A
|
NP_001358585.1:p.Gln1279Lys
|
|
NM_001374820.1:c.3835C>A
|
NP_001361749.1:p.Gln1279Lys
|
|
NM_001374828.1:c.3955C>A
MANE Select
|
NP_001361757.1:p.Gln1319Lys
|
|
NM_017519.3:c.3796C>A
|
NP_059989.3:p.Gln1266Lys
|
|