ENST00000375412.11:c.738A>T
MANE Select
|
ENSP00000364561.5:p.Pro246=
|
|
ENST00000649557.1:c.192A>T
|
ENSP00000496904.1:p.Pro64=
|
|
ENST00000650398.1:n.761A>T
|
|
|
ENST00000375412.9:c.738A>T
|
ENSP00000364561.5:p.Pro246=
|
|
ENST00000423591.5:c.192A>T
|
ENSP00000414298.1:p.Pro64=
|
|
ENST00000428152.1:n.454A>T
|
|
|
ENST00000428378.1:c.189A>T
|
ENSP00000416978.1:p.Pro63=
|
|
ENST00000476484.5:c.*136A>T
|
ENSP00000429212.1:n.*136A>T
|
|
ENST00000479094.5:n.755A>T
|
|
|
ENST00000483056.5:n.560A>T
|
|
|
ENST00000483149.6:n.693A>T
|
|
|
ENST00000520403.1:n.735A>T
|
|
|
ENST00000520470.5:n.814A>T
|
|
|
ENST00000523407.1:n.616A>T
|
|
|
NM_198841.2:c.738A>T
|
NP_942138.2:p.Pro246=
|
|
XM_005251736.2:c.825A>T
|
XP_005251793.1:p.Pro275=
|
|
NM_001322224.2:c.192A>T
|
NP_001309153.1:p.Pro64=
|
|
NM_198841.3:c.738A>T
|
NP_942138.2:p.Pro246=
|
|
NR_136229.2:n.1037A>T
|
|
|
NR_136230.2:n.1158A>T
|
|
|
NR_136231.2:n.1751A>T
|
|
|
NR_136232.2:n.963A>T
|
|
|
NR_136233.2:n.786A>T
|
|
|
NR_136234.2:n.820A>T
|
|
|
NR_136235.2:n.842A>T
|
|
|
NR_136236.2:n.1045A>T
|
|
|
NR_136237.2:n.1166A>T
|
|
|
NR_136238.2:n.907A>T
|
|
|
NM_198841.4:c.738A>T
MANE Select
|
NP_942138.2:p.Pro246=
|
|
NM_001322224.3:c.192A>T
|
NP_001309153.1:p.Pro64=
|
|
NR_136231.3:n.1731A>T
|
|
|
NR_136232.3:n.960A>T
|
|
|
NR_136233.3:n.783A>T
|
|
|
NR_136234.3:n.817A>T
|
|
|
NR_136235.3:n.839A>T
|
|
|
NR_136236.3:n.1042A>T
|
|
|
NR_136237.3:n.1163A>T
|
|
|
NR_136238.3:n.904A>T
|
|
|