ENST00000254108.12:c.1566G>T
MANE Select
|
ENSP00000254108.8:p.Arg522Ser
|
|
ENST00000254108.11:c.1566G>T
|
ENSP00000254108.7:p.Arg522Ser
|
|
ENST00000380244.7:c.1563G>T
|
ENSP00000369594.3:p.Arg521Ser
|
|
ENST00000483853.1:n.643G>T
|
|
|
ENST00000487509.6:n.4741G>T
|
|
|
ENST00000566605.5:c.*739G>T
|
ENSP00000455073.1:n.*739G>T
|
|
ENST00000568685.1:c.1569G>T
|
ENSP00000455282.1:p.Arg523Ser
|
|
ENST00000569760.5:n.457G>T
|
|
|
NM_001170634.1:c.1563G>T
|
NP_001164105.1:p.Arg521Ser
|
|
NM_001170937.1:c.1554G>T
|
NP_001164408.1:p.Arg518Ser
|
|
NM_004960.3:c.1566G>T , LRG_655t1:c.1566G>T
|
NP_004951.1:p.Arg522Ser
|
|
NR_028388.2:n.1636G>T
|
|
|
XM_005255233.3:c.951G>T
|
XP_005255290.1:p.Arg317Ser
|
|
XM_011545781.1:c.1560G>T
|
XP_011544083.1:p.Arg520Ser
|
|
XM_011545782.1:c.951G>T
|
XP_011544084.1:p.Arg317Ser
|
|
XM_005255233.5:c.951G>T
|
XP_005255290.1:p.Arg317Ser
|
|
XM_011545782.2:c.951G>T
|
XP_011544084.1:p.Arg317Ser
|
|
XM_024450221.1:c.1557G>T
|
XP_024305989.1:p.Arg519Ser
|
|
NM_004960.4:c.1566G>T
MANE Select
|
NP_004951.1:p.Arg522Ser
|
|