ENST00000350026.11:c.3039G>A
|
ENSP00000055163.8:p.Gln1013=
|
|
ENST00000414678.8:c.2949G>A
|
ENSP00000412835.3:p.Gln983=
|
|
ENST00000637015.2:c.3039G>A
|
ENSP00000489729.2:p.Gln1013=
|
|
ENST00000319584.11:c.1053G>A
|
ENSP00000313006.7:p.Gln351=
|
|
ENST00000346085.10:c.3078G>A
|
ENSP00000344546.5:p.Gln1026=
|
|
ENST00000350026.10:c.2790G>A
|
ENSP00000055163.7:p.Gln930=
|
|
ENST00000414678.7:c.1197G>A
|
ENSP00000412835.2:p.Gln399=
|
|
ENST00000452544.2:n.940G>A
|
|
|
ENST00000635849.1:c.360G>A
|
ENSP00000490948.1:p.Gln120=
|
|
ENST00000636426.1:n.173G>A
|
|
|
ENST00000636930.2:c.3039G>A
MANE Select
|
ENSP00000490491.2:p.Gln1013=
|
|
ENST00000637015.1:c.278G>A
|
|
|
ENST00000637568.1:c.82G>A
|
|
|
ENST00000637810.1:c.540G>A
|
ENSP00000489636.1:p.Gln180=
|
|
ENST00000637904.1:c.540G>A
|
ENSP00000490550.1:p.Gln180=
|
|
ENST00000647938.1:c.2829G>A
|
ENSP00000498155.1:p.Gln943=
|
|
ENST00000674190.1:n.1788G>A
|
|
|
ENST00000319584.10:c.1056G>A
|
ENSP00000313006.6:p.Gln352=
|
|
ENST00000346085.9:c.2829G>A
|
ENSP00000344546.4:p.Gln943=
|
|
ENST00000350026.9:c.2790G>A
|
ENSP00000055163.7:p.Gln930=
|
|
ENST00000414678.6:c.1197G>A
|
ENSP00000412835.2:p.Gln399=
|
|
ENST00000452544.1:n.886G>A
|
|
|
ENST00000478761.3:c.112G>A
|
|
|
NM_017519.2:c.2790G>A
|
NP_059989.2:p.Gln930=
|
|
NM_020732.3:c.2829G>A
|
NP_065783.3:p.Gln943=
|
|
XM_005267069.3:c.2790G>A
|
XP_005267126.2:p.Gln930=
|
|
XM_011535984.1:c.1740G>A
|
XP_011534286.1:p.Gln580=
|
|
XM_011535985.1:c.1560G>A
|
XP_011534287.1:p.Gln520=
|
|
XM_011535986.1:c.1320G>A
|
XP_011534288.1:p.Gln440=
|
|
XM_011535987.1:c.939G>A
|
XP_011534289.1:p.Gln313=
|
|
XM_011535988.1:c.-20+15694G>A
|
XP_011534290.1:n.-20+15694G>A
|
|
NM_001346813.1:c.2790G>A
|
NP_001333742.1:p.Gln930=
|
|
NM_001363725.1:c.540G>A
|
NP_001350654.1:p.Gln180=
|
|
XM_011535984.2:c.2871G>A
|
XP_011534286.2:p.Gln957=
|
|
XM_011535988.3:c.-20+15694G>A
|
XP_011534290.1:n.-20+15694G>A
|
|
XM_017011103.2:c.2871G>A
|
XP_016866592.1:p.Gln957=
|
|
XM_017011104.1:c.2871G>A
|
XP_016866593.1:p.Gln957=
|
|
XM_017011105.2:c.2871G>A
|
XP_016866594.1:p.Gln957=
|
|
XM_017011106.2:c.2871G>A
|
XP_016866595.1:p.Gln957=
|
|
XM_017011107.2:c.2691G>A
|
XP_016866596.1:p.Gln897=
|
|
XR_002956289.1:n.2954G>A
|
|
|
NM_001363725.2:c.540G>A
|
NP_001350654.1:p.Gln180=
|
|
NM_001371656.1:c.3078G>A
|
NP_001358585.1:p.Gln1026=
|
|
NM_001374820.1:c.3078G>A
|
NP_001361749.1:p.Gln1026=
|
|
NM_001374828.1:c.3039G>A
MANE Select
|
NP_001361757.1:p.Gln1013=
|
|
NM_017519.3:c.3039G>A
|
NP_059989.3:p.Gln1013=
|
|