ENST00000350026.11:c.3054A>C
|
ENSP00000055163.8:p.Ala1018=
|
|
ENST00000414678.8:c.2964A>C
|
ENSP00000412835.3:p.Ala988=
|
|
ENST00000637015.2:c.3054A>C
|
ENSP00000489729.2:p.Ala1018=
|
|
ENST00000319584.11:c.1068A>C
|
ENSP00000313006.7:p.Ala356=
|
|
ENST00000346085.10:c.3093A>C
|
ENSP00000344546.5:p.Ala1031=
|
|
ENST00000350026.10:c.2805A>C
|
ENSP00000055163.7:p.Ala935=
|
|
ENST00000414678.7:c.1212A>C
|
ENSP00000412835.2:p.Ala404=
|
|
ENST00000452544.2:n.955A>C
|
|
|
ENST00000635849.1:c.375A>C
|
ENSP00000490948.1:p.Ala125=
|
|
ENST00000635957.1:c.9A>C
|
ENSP00000490385.1:p.Ala3=
|
|
ENST00000636426.1:n.188A>C
|
|
|
ENST00000636930.2:c.3054A>C
MANE Select
|
ENSP00000490491.2:p.Ala1018=
|
|
ENST00000637015.1:c.293A>C
|
|
|
ENST00000637568.1:c.97A>C
|
|
|
ENST00000637810.1:c.555A>C
|
ENSP00000489636.1:p.Ala185=
|
|
ENST00000637904.1:c.555A>C
|
ENSP00000490550.1:p.Ala185=
|
|
ENST00000647938.1:c.2844A>C
|
ENSP00000498155.1:p.Ala948=
|
|
ENST00000674190.1:n.1803A>C
|
|
|
ENST00000319584.10:c.1071A>C
|
ENSP00000313006.6:p.Ala357=
|
|
ENST00000346085.9:c.2844A>C
|
ENSP00000344546.4:p.Ala948=
|
|
ENST00000350026.9:c.2805A>C
|
ENSP00000055163.7:p.Ala935=
|
|
ENST00000400790.3:c.6A>C
|
ENSP00000383596.3:p.Ala2=
|
|
ENST00000414678.6:c.1212A>C
|
ENSP00000412835.2:p.Ala404=
|
|
ENST00000452544.1:n.901A>C
|
|
|
ENST00000478761.3:c.127A>C
|
|
|
NM_017519.2:c.2805A>C
|
NP_059989.2:p.Ala935=
|
|
NM_020732.3:c.2844A>C
|
NP_065783.3:p.Ala948=
|
|
XM_005267069.3:c.2805A>C
|
XP_005267126.2:p.Ala935=
|
|
XM_011535984.1:c.1755A>C
|
XP_011534286.1:p.Ala585=
|
|
XM_011535985.1:c.1575A>C
|
XP_011534287.1:p.Ala525=
|
|
XM_011535986.1:c.1335A>C
|
XP_011534288.1:p.Ala445=
|
|
XM_011535987.1:c.954A>C
|
XP_011534289.1:p.Ala318=
|
|
XM_011535988.1:c.-20+15709A>C
|
XP_011534290.1:n.-20+15709A>C
|
|
NM_001346813.1:c.2805A>C
|
NP_001333742.1:p.Ala935=
|
|
NM_001363725.1:c.555A>C
|
NP_001350654.1:p.Ala185=
|
|
XM_011535984.2:c.2886A>C
|
XP_011534286.2:p.Ala962=
|
|
XM_011535988.3:c.-20+15709A>C
|
XP_011534290.1:n.-20+15709A>C
|
|
XM_017011103.2:c.2886A>C
|
XP_016866592.1:p.Ala962=
|
|
XM_017011104.1:c.2886A>C
|
XP_016866593.1:p.Ala962=
|
|
XM_017011105.2:c.2886A>C
|
XP_016866594.1:p.Ala962=
|
|
XM_017011106.2:c.2886A>C
|
XP_016866595.1:p.Ala962=
|
|
XM_017011107.2:c.2706A>C
|
XP_016866596.1:p.Ala902=
|
|
XR_002956289.1:n.2969A>C
|
|
|
NM_001363725.2:c.555A>C
|
NP_001350654.1:p.Ala185=
|
|
NM_001371656.1:c.3093A>C
|
NP_001358585.1:p.Ala1031=
|
|
NM_001374820.1:c.3093A>C
|
NP_001361749.1:p.Ala1031=
|
|
NM_001374828.1:c.3054A>C
MANE Select
|
NP_001361757.1:p.Ala1018=
|
|
NM_017519.3:c.3054A>C
|
NP_059989.3:p.Ala1018=
|
|