ENST00000432791.7:c.3022G>A
MANE Select
|
ENSP00000387393.3:p.Asp1008Asn
|
|
ENST00000572904.6:c.3022G>A
|
ENSP00000461484.1:p.Asp1008Asn
|
|
ENST00000574590.6:c.3019G>A
|
ENSP00000461812.2:p.Asp1007Asn
|
|
ENST00000575318.6:c.2830G>A
|
ENSP00000461299.1:p.Asp944Asn
|
|
ENST00000638275.1:c.2830G>A
|
ENSP00000492576.1:p.Asp944Asn
|
|
ENST00000639805.1:n.439G>A
|
|
|
ENST00000648792.1:c.2890G>A
|
ENSP00000497628.1:p.Asp964Asn
|
|
ENST00000262419.10:c.3022G>A
|
ENSP00000262419.6:p.Asp1008Asn
|
|
ENST00000432791.5:c.3019G>A
|
ENSP00000387393.2:p.Asp1007Asn
|
|
ENST00000572218.5:n.7239G>A
|
|
|
ENST00000572904.5:c.3022G>A
|
ENSP00000461484.1:p.Asp1008Asn
|
|
ENST00000574590.5:c.3022G>A
|
ENSP00000461812.1:p.Asp1008Asn
|
|
ENST00000574963.1:n.452G>A
|
|
|
ENST00000575318.5:c.2830G>A
|
ENSP00000461299.1:p.Asp944Asn
|
|
ENST00000576870.5:n.994G>A
|
|
|
NM_001193465.1:c.3019G>A
|
NP_001180394.1:p.Asp1007Asn
|
|
NM_001193466.1:c.3022G>A
|
NP_001180395.1:p.Asp1008Asn
|
|
NM_015443.3:c.3022G>A
|
NP_056258.1:p.Asp1008Asn
|
|
XM_006721823.1:c.3022G>A
|
XP_006721886.1:p.Asp1008Asn
|
|
XM_006721824.2:c.3022G>A
|
XP_006721887.1:p.Asp1008Asn
|
|
XM_011524628.1:c.3019G>A
|
XP_011522930.1:p.Asp1007Asn
|
|
XM_011524629.1:c.2920G>A
|
XP_011522931.1:p.Asp974Asn
|
|
XM_011524630.1:c.2833G>A
|
XP_011522932.1:p.Asp945Asn
|
|
XM_011524631.1:c.2830G>A
|
XP_011522933.1:p.Asp944Asn
|
|
XM_011524632.1:c.1792G>A
|
XP_011522934.1:p.Asp598Asn
|
|
XM_006721823.2:c.3022G>A
|
XP_006721886.1:p.Asp1008Asn
|
|
XM_006721824.4:c.3022G>A
|
XP_006721887.1:p.Asp1008Asn
|
|
XM_011524628.3:c.3019G>A
|
XP_011522930.1:p.Asp1007Asn
|
|
XM_011524629.3:c.2920G>A
|
XP_011522931.1:p.Asp974Asn
|
|
XM_011524630.3:c.2833G>A
|
XP_011522932.1:p.Asp945Asn
|
|
XM_011524631.3:c.2830G>A
|
XP_011522933.1:p.Asp944Asn
|
|
XM_011524632.3:c.1792G>A
|
XP_011522934.1:p.Asp598Asn
|
|
XM_017024488.2:c.2830G>A
|
XP_016879977.1:p.Asp944Asn
|
|
NM_001193466.2:c.3022G>A
|
NP_001180395.1:p.Asp1008Asn
|
|
NM_015443.4:c.3022G>A
MANE Select
|
NP_056258.1:p.Asp1008Asn
|
|
NM_001193465.2:c.3019G>A
|
NP_001180394.1:p.Asp1007Asn
|
|
NM_001379198.1:c.3022G>A
|
NP_001366127.1:p.Asp1008Asn
|
|