ENST00000254108.12:c.910T>A
MANE Select
|
ENSP00000254108.8:p.Tyr304Asn
|
|
ENST00000254108.11:c.910T>A
|
ENSP00000254108.7:p.Tyr304Asn
|
|
ENST00000380244.7:c.907T>A
|
ENSP00000369594.3:p.Tyr303Asn
|
|
ENST00000474990.5:n.204T>A
|
|
|
ENST00000487509.6:n.4085T>A
|
|
|
ENST00000564766.1:n.734T>A
|
|
|
ENST00000566605.5:c.*83T>A
|
ENSP00000455073.1:n.*83T>A
|
|
ENST00000568685.1:c.913T>A
|
ENSP00000455282.1:p.Tyr305Asn
|
|
ENST00000568901.2:n.284T>A
|
|
|
NM_001170634.1:c.907T>A
|
NP_001164105.1:p.Tyr303Asn
|
|
NM_001170937.1:c.898T>A
|
NP_001164408.1:p.Tyr300Asn
|
|
NM_004960.3:c.910T>A , LRG_655t1:c.910T>A
|
NP_004951.1:p.Tyr304Asn
|
|
NR_028388.2:n.980T>A
|
|
|
XM_005255233.3:c.295T>A
|
XP_005255290.1:p.Tyr99Asn
|
|
XM_011545781.1:c.904T>A
|
XP_011544083.1:p.Tyr302Asn
|
|
XM_011545782.1:c.295T>A
|
XP_011544084.1:p.Tyr99Asn
|
|
XM_005255233.5:c.295T>A
|
XP_005255290.1:p.Tyr99Asn
|
|
XM_011545782.2:c.295T>A
|
XP_011544084.1:p.Tyr99Asn
|
|
XM_024450221.1:c.901T>A
|
XP_024305989.1:p.Tyr301Asn
|
|
NM_004960.4:c.910T>A
MANE Select
|
NP_004951.1:p.Tyr304Asn
|
|