ENST00000436117.3:c.*616G>A
|
ENSP00000410980.2:n.*616G>A
|
|
ENST00000318493.11:c.3065G>A
|
ENSP00000317272.6:p.Arg1022Gln
|
|
ENST00000397752.8:c.3011G>A
MANE Select
|
ENSP00000380860.3:p.Arg1004Gln
|
|
ENST00000318493.10:c.3065G>A
|
ENSP00000317272.6:p.Arg1022Gln
|
|
ENST00000397752.7:c.3011G>A
|
ENSP00000380860.3:p.Arg1004Gln
|
|
ENST00000454623.1:c.283+318G>A
|
ENSP00000398140.1:n.283+318G>A
|
|
NM_000245.2:c.3011G>A
|
NP_000236.2:p.Arg1004Gln
|
|
NM_001127500.1:c.3065G>A , LRG_662t1:c.3065G>A
|
NP_001120972.1:p.Arg1022Gln
|
|
XM_006715990.2:c.1721G>A
|
XP_006716053.1:p.Arg574Gln
|
|
XM_006715991.2:c.1721G>A
|
XP_006716054.1:p.Arg574Gln
|
|
XM_011516223.1:c.3068G>A
|
XP_011514525.1:p.Arg1023Gln
|
|
NM_000245.3:c.3011G>A
|
NP_000236.2:p.Arg1004Gln
|
|
NM_001127500.2:c.3065G>A
|
NP_001120972.1:p.Arg1022Gln
|
|
NM_001324402.1:c.1721G>A
|
NP_001311331.1:p.Arg574Gln
|
|
XR_001744772.1:n.3142G>A
|
|
|
NM_001127500.3:c.3065G>A
|
NP_001120972.1:p.Arg1022Gln
|
|
NM_000245.4:c.3011G>A
MANE Select
|
NP_000236.2:p.Arg1004Gln
|
|
NM_001324402.2:c.1721G>A
|
NP_001311331.1:p.Arg574Gln
|
|