ENST00000328194.8:c.3547A>T
MANE Select
|
ENSP00000328524.3:p.Asn1183Tyr
|
|
ENST00000525784.6:n.1409A>T
|
|
|
ENST00000530780.2:c.*3373A>T
|
ENSP00000433925.1:n.*3373A>T
|
|
ENST00000531747.2:n.3218A>T
|
|
|
ENST00000679446.1:n.3468A>T
|
|
|
ENST00000679458.1:n.4948A>T
|
|
|
ENST00000679460.1:n.4609A>T
|
|
|
ENST00000679568.1:c.3547A>T
|
ENSP00000505860.1:p.Asn1183Tyr
|
|
ENST00000679745.1:n.4052A>T
|
|
|
ENST00000679773.1:n.2708A>T
|
|
|
ENST00000679926.1:n.4849A>T
|
|
|
ENST00000679999.1:c.*604A>T
|
ENSP00000505198.1:n.*604A>T
|
|
ENST00000680252.1:c.3214A>T
|
|
|
ENST00000680294.1:c.3340A>T
|
ENSP00000506113.1:p.Asn1114Tyr
|
|
ENST00000680358.1:n.2846A>T
|
|
|
ENST00000680470.1:c.*1328A>T
|
ENSP00000505975.1:n.*1328A>T
|
|
ENST00000680554.1:c.*80A>T
|
ENSP00000505621.1:n.*80A>T
|
|
ENST00000680576.1:n.5023A>T
|
|
|
ENST00000680599.1:n.3588A>T
|
|
|
ENST00000680742.1:c.*80A>T
|
ENSP00000505206.1:n.*80A>T
|
|
ENST00000680791.1:n.2431A>T
|
|
|
ENST00000680885.1:n.5249A>T
|
|
|
ENST00000681158.1:c.3131A>T
|
|
|
ENST00000681203.1:c.3475A>T
|
ENSP00000506456.1:p.Asn1159Tyr
|
|
ENST00000681371.1:n.3419A>T
|
|
|
ENST00000681425.1:n.4025A>T
|
|
|
ENST00000681639.1:n.1826A>T
|
|
|
ENST00000328194.7:c.3547A>T
|
ENSP00000328524.3:p.Asn1183Tyr
|
|
ENST00000525784.5:c.483A>T
|
|
|
ENST00000527700.5:n.3109A>T
|
|
|
ENST00000528725.5:c.243A>T
|
|
|
ENST00000529977.5:n.1448A>T
|
|
|
ENST00000530044.5:c.3547A>T
|
ENSP00000435866.1:p.Asn1183Tyr
|
|
ENST00000531747.1:c.783A>T
|
|
|
ENST00000533737.5:c.210A>T
|
|
|
NM_001243254.1:c.3547A>T
|
NP_001230183.1:p.Asn1183Tyr
|
|
NM_015213.3:c.3547A>T
|
NP_056028.2:p.Asn1183Tyr
|
|
XM_005252832.1:c.3547A>T
|
XP_005252889.1:p.Asn1183Tyr
|
|
XM_011519952.1:c.3547A>T
|
XP_011518254.1:p.Asn1183Tyr
|
|
XM_011519953.1:c.1645A>T
|
XP_011518255.1:p.Asn549Tyr
|
|
XR_242782.2:n.3729A>T
|
|
|
XR_930851.1:n.3729A>T
|
|
|
NM_001348749.1:c.3475A>T
|
NP_001335678.1:p.Asn1159Tyr
|
|
NM_001348750.1:c.3259A>T
|
NP_001335679.1:p.Asn1087Tyr
|
|
NR_145966.2:n.3721A>T
|
|
|
NM_015213.4:c.3547A>T
MANE Select
|
NP_056028.2:p.Asn1183Tyr
|
|
NM_001243254.2:c.3547A>T
|
NP_001230183.1:p.Asn1183Tyr
|
|
NM_001348749.2:c.3475A>T
|
NP_001335678.1:p.Asn1159Tyr
|
|
NM_001348750.2:c.3259A>T
|
NP_001335679.1:p.Asn1087Tyr
|
|