ENST00000328194.8:c.3588G>A
MANE Select
|
ENSP00000328524.3:p.Arg1196=
|
|
ENST00000525784.6:n.1450G>A
|
|
|
ENST00000530780.2:c.*3414G>A
|
ENSP00000433925.1:n.*3414G>A
|
|
ENST00000531747.2:n.3259G>A
|
|
|
ENST00000679446.1:n.3509G>A
|
|
|
ENST00000679458.1:n.4989G>A
|
|
|
ENST00000679460.1:n.4650G>A
|
|
|
ENST00000679568.1:c.3588G>A
|
ENSP00000505860.1:p.Arg1196=
|
|
ENST00000679745.1:n.4093G>A
|
|
|
ENST00000679773.1:n.2749G>A
|
|
|
ENST00000679926.1:n.4890G>A
|
|
|
ENST00000679999.1:c.*645G>A
|
ENSP00000505198.1:n.*645G>A
|
|
ENST00000680252.1:c.3255G>A
|
|
|
ENST00000680294.1:c.3381G>A
|
ENSP00000506113.1:p.Arg1127=
|
|
ENST00000680358.1:n.2887G>A
|
|
|
ENST00000680470.1:c.*1369G>A
|
ENSP00000505975.1:n.*1369G>A
|
|
ENST00000680554.1:c.*121G>A
|
ENSP00000505621.1:n.*121G>A
|
|
ENST00000680576.1:n.5064G>A
|
|
|
ENST00000680599.1:n.3629G>A
|
|
|
ENST00000680742.1:c.*121G>A
|
ENSP00000505206.1:n.*121G>A
|
|
ENST00000680791.1:n.2472G>A
|
|
|
ENST00000680885.1:n.5290G>A
|
|
|
ENST00000681158.1:c.3172G>A
|
|
|
ENST00000681203.1:c.3516G>A
|
ENSP00000506456.1:p.Arg1172=
|
|
ENST00000681371.1:n.3460G>A
|
|
|
ENST00000681425.1:n.4066G>A
|
|
|
ENST00000681639.1:n.1867G>A
|
|
|
ENST00000328194.7:c.3588G>A
|
ENSP00000328524.3:p.Arg1196=
|
|
ENST00000525784.5:c.524G>A
|
|
|
ENST00000527700.5:n.3150G>A
|
|
|
ENST00000528725.5:c.284G>A
|
|
|
ENST00000529977.5:n.1489G>A
|
|
|
ENST00000530044.5:c.3588G>A
|
ENSP00000435866.1:p.Arg1196=
|
|
ENST00000531747.1:c.824G>A
|
|
|
ENST00000533737.5:c.251G>A
|
|
|
NM_001243254.1:c.3588G>A
|
NP_001230183.1:p.Arg1196=
|
|
NM_015213.3:c.3588G>A
|
NP_056028.2:p.Arg1196=
|
|
XM_005252832.1:c.3588G>A
|
XP_005252889.1:p.Arg1196=
|
|
XM_011519952.1:c.3588G>A
|
XP_011518254.1:p.Arg1196=
|
|
XM_011519953.1:c.1686G>A
|
XP_011518255.1:p.Arg562=
|
|
XR_242782.2:n.3770G>A
|
|
|
XR_930851.1:n.3770G>A
|
|
|
NM_001348749.1:c.3516G>A
|
NP_001335678.1:p.Arg1172=
|
|
NM_001348750.1:c.3300G>A
|
NP_001335679.1:p.Arg1100=
|
|
NR_145966.2:n.3762G>A
|
|
|
NM_015213.4:c.3588G>A
MANE Select
|
NP_056028.2:p.Arg1196=
|
|
NM_001243254.2:c.3588G>A
|
NP_001230183.1:p.Arg1196=
|
|
NM_001348749.2:c.3516G>A
|
NP_001335678.1:p.Arg1172=
|
|
NM_001348750.2:c.3300G>A
|
NP_001335679.1:p.Arg1100=
|
|