ENST00000254108.12:c.1565G>C
MANE Select
|
ENSP00000254108.8:p.Arg522Thr
|
|
ENST00000254108.11:c.1565G>C
|
ENSP00000254108.7:p.Arg522Thr
|
|
ENST00000380244.7:c.1562G>C
|
ENSP00000369594.3:p.Arg521Thr
|
|
ENST00000483853.1:n.642G>C
|
|
|
ENST00000487509.6:n.4740G>C
|
|
|
ENST00000566605.5:c.*738G>C
|
ENSP00000455073.1:n.*738G>C
|
|
ENST00000568685.1:c.1568G>C
|
ENSP00000455282.1:p.Arg523Thr
|
|
ENST00000569760.5:n.456G>C
|
|
|
NM_001170634.1:c.1562G>C
|
NP_001164105.1:p.Arg521Thr
|
|
NM_001170937.1:c.1553G>C
|
NP_001164408.1:p.Arg518Thr
|
|
NM_004960.3:c.1565G>C , LRG_655t1:c.1565G>C
|
NP_004951.1:p.Arg522Thr
|
|
NR_028388.2:n.1635G>C
|
|
|
XM_005255233.3:c.950G>C
|
XP_005255290.1:p.Arg317Thr
|
|
XM_011545781.1:c.1559G>C
|
XP_011544083.1:p.Arg520Thr
|
|
XM_011545782.1:c.950G>C
|
XP_011544084.1:p.Arg317Thr
|
|
XM_005255233.5:c.950G>C
|
XP_005255290.1:p.Arg317Thr
|
|
XM_011545782.2:c.950G>C
|
XP_011544084.1:p.Arg317Thr
|
|
XM_024450221.1:c.1556G>C
|
XP_024305989.1:p.Arg519Thr
|
|
NM_004960.4:c.1565G>C
MANE Select
|
NP_004951.1:p.Arg522Thr
|
|