ENST00000254108.12:c.1565G>T
MANE Select
|
ENSP00000254108.8:p.Arg522Met
|
|
ENST00000254108.11:c.1565G>T
|
ENSP00000254108.7:p.Arg522Met
|
|
ENST00000380244.7:c.1562G>T
|
ENSP00000369594.3:p.Arg521Met
|
|
ENST00000483853.1:n.642G>T
|
|
|
ENST00000487509.6:n.4740G>T
|
|
|
ENST00000566605.5:c.*738G>T
|
ENSP00000455073.1:n.*738G>T
|
|
ENST00000568685.1:c.1568G>T
|
ENSP00000455282.1:p.Arg523Met
|
|
ENST00000569760.5:n.456G>T
|
|
|
NM_001170634.1:c.1562G>T
|
NP_001164105.1:p.Arg521Met
|
|
NM_001170937.1:c.1553G>T
|
NP_001164408.1:p.Arg518Met
|
|
NM_004960.3:c.1565G>T , LRG_655t1:c.1565G>T
|
NP_004951.1:p.Arg522Met
|
|
NR_028388.2:n.1635G>T
|
|
|
XM_005255233.3:c.950G>T
|
XP_005255290.1:p.Arg317Met
|
|
XM_011545781.1:c.1559G>T
|
XP_011544083.1:p.Arg520Met
|
|
XM_011545782.1:c.950G>T
|
XP_011544084.1:p.Arg317Met
|
|
XM_005255233.5:c.950G>T
|
XP_005255290.1:p.Arg317Met
|
|
XM_011545782.2:c.950G>T
|
XP_011544084.1:p.Arg317Met
|
|
XM_024450221.1:c.1556G>T
|
XP_024305989.1:p.Arg519Met
|
|
NM_004960.4:c.1565G>T
MANE Select
|
NP_004951.1:p.Arg522Met
|
|