ENST00000254108.12:c.883A>T
MANE Select
|
ENSP00000254108.8:p.Asn295Tyr
|
|
ENST00000254108.11:c.883A>T
|
ENSP00000254108.7:p.Asn295Tyr
|
|
ENST00000380244.7:c.880A>T
|
ENSP00000369594.3:p.Asn294Tyr
|
|
ENST00000474990.5:n.177A>T
|
|
|
ENST00000487509.6:n.4058A>T
|
|
|
ENST00000564766.1:n.707A>T
|
|
|
ENST00000566605.5:c.*56A>T
|
ENSP00000455073.1:n.*56A>T
|
|
ENST00000568685.1:c.886A>T
|
ENSP00000455282.1:p.Asn296Tyr
|
|
ENST00000568901.2:n.257A>T
|
|
|
NM_001170634.1:c.880A>T
|
NP_001164105.1:p.Asn294Tyr
|
|
NM_001170937.1:c.871A>T
|
NP_001164408.1:p.Asn291Tyr
|
|
NM_004960.3:c.883A>T , LRG_655t1:c.883A>T
|
NP_004951.1:p.Asn295Tyr
|
|
NR_028388.2:n.953A>T
|
|
|
XM_005255233.3:c.268A>T
|
XP_005255290.1:p.Asn90Tyr
|
|
XM_011545781.1:c.877A>T
|
XP_011544083.1:p.Asn293Tyr
|
|
XM_011545782.1:c.268A>T
|
XP_011544084.1:p.Asn90Tyr
|
|
XM_005255233.5:c.268A>T
|
XP_005255290.1:p.Asn90Tyr
|
|
XM_011545782.2:c.268A>T
|
XP_011544084.1:p.Asn90Tyr
|
|
XM_024450221.1:c.874A>T
|
XP_024305989.1:p.Asn292Tyr
|
|
NM_004960.4:c.883A>T
MANE Select
|
NP_004951.1:p.Asn295Tyr
|
|