ENST00000350026.11:c.3406G=
|
ENSP00000055163.8:p.Glu1136=
|
|
ENST00000414678.8:c.3475G=
|
ENSP00000412835.3:p.Glu1159=
|
|
ENST00000637015.2:c.3694G=
|
ENSP00000489729.2:p.Glu1232=
|
|
ENST00000319584.11:c.1579G=
|
ENSP00000313006.7:p.Glu527=
|
|
ENST00000346085.10:c.3445G=
|
ENSP00000344546.5:p.Glu1149=
|
|
ENST00000350026.10:c.3157G=
|
ENSP00000055163.7:p.Glu1053=
|
|
ENST00000414678.7:c.1723G=
|
ENSP00000412835.2:p.Glu575=
|
|
ENST00000635849.1:c.886G=
|
ENSP00000490948.1:p.Glu296=
|
|
ENST00000635957.1:c.520G=
|
ENSP00000490385.1:p.Glu174=
|
|
ENST00000636930.2:c.3565G=
MANE Select
|
ENSP00000490491.2:p.Glu1189=
|
|
ENST00000636940.1:n.1562G=
|
|
|
ENST00000637015.1:c.933G=
|
|
|
ENST00000637568.1:c.847G=
|
|
|
ENST00000637741.1:n.231G=
|
|
|
ENST00000637810.1:c.907G=
|
ENSP00000489636.1:p.Glu303=
|
|
ENST00000637904.1:c.1066G=
|
ENSP00000490550.1:p.Glu356=
|
|
ENST00000647938.1:c.3196G=
|
ENSP00000498155.1:p.Glu1066=
|
|
ENST00000319584.10:c.1582G=
|
ENSP00000313006.6:p.Glu528=
|
|
ENST00000346085.9:c.3196G=
|
ENSP00000344546.4:p.Glu1066=
|
|
ENST00000350026.9:c.3157G=
|
ENSP00000055163.7:p.Glu1053=
|
|
ENST00000400790.3:c.358G=
|
ENSP00000383596.3:p.Glu120=
|
|
ENST00000414678.6:c.1723G=
|
ENSP00000412835.2:p.Glu575=
|
|
ENST00000478761.3:c.767G=
|
|
|
NM_017519.2:c.3157G=
|
NP_059989.2:p.Glu1053=
|
|
NM_020732.3:c.3196G=
|
NP_065783.3:p.Glu1066=
|
|
XM_005267069.3:c.3316G=
|
XP_005267126.2:p.Glu1106=
|
|
XM_011535984.1:c.2395G=
|
XP_011534286.1:p.Glu799=
|
|
XM_011535985.1:c.2215G=
|
XP_011534287.1:p.Glu739=
|
|
XM_011535986.1:c.1975G=
|
XP_011534288.1:p.Glu659=
|
|
XM_011535987.1:c.1594G=
|
XP_011534289.1:p.Glu532=
|
|
XM_011535988.1:c.457G=
|
XP_011534290.1:p.Glu153=
|
|
NM_001346813.1:c.3316G=
|
NP_001333742.1:p.Glu1106=
|
|
NM_001363725.1:c.1066G=
|
NP_001350654.1:p.Glu356=
|
|
XM_011535984.2:c.3526G=
|
XP_011534286.2:p.Glu1176=
|
|
XM_011535988.3:c.457G=
|
XP_011534290.1:p.Glu153=
|
|
XM_017011103.2:c.3427G=
|
XP_016866592.1:p.Glu1143=
|
|
XM_017011104.1:c.3397G=
|
XP_016866593.1:p.Glu1133=
|
|
XM_017011105.2:c.3367G=
|
XP_016866594.1:p.Glu1123=
|
|
XM_017011106.2:c.3238G=
|
XP_016866595.1:p.Glu1080=
|
|
XM_017011107.2:c.3217G=
|
XP_016866596.1:p.Glu1073=
|
|
XR_002956289.1:n.3609G=
|
|
|
NM_001363725.2:c.1066G=
|
NP_001350654.1:p.Glu356=
|
|
NM_001371656.1:c.3445G=
|
NP_001358585.1:p.Glu1149=
|
|
NM_001374820.1:c.3445G=
|
NP_001361749.1:p.Glu1149=
|
|
NM_001374828.1:c.3565G=
MANE Select
|
NP_001361757.1:p.Glu1189=
|
|
NM_017519.3:c.3406G=
|
NP_059989.3:p.Glu1136=
|
|