ENST00000409959.8:c.4631A>C
MANE Select
|
ENSP00000386787.3:p.Asp1544Ala
|
|
ENST00000240487.5:c.3962A>C
|
ENSP00000240487.5:p.Asp1321Ala
|
|
ENST00000409663.7:c.4628A>C
|
ENSP00000386574.3:p.Asp1543Ala
|
|
ENST00000409959.7:c.4631A>C
|
ENSP00000386787.3:p.Asp1544Ala
|
|
NM_001131007.1:c.4631A>C
|
NP_001124479.1:p.Asp1544Ala
|
|
NM_015196.3:c.4628A>C
|
NP_056011.3:p.Asp1543Ala
|
|
XM_005262871.3:c.2753A>C
|
XP_005262928.2:p.Asp918Ala
|
|
XM_011531780.1:c.4718A>C
|
XP_011530082.1:p.Asp1573Ala
|
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XM_011531781.1:c.4715A>C
|
XP_011530083.1:p.Asp1572Ala
|
|
XM_011531782.1:c.4688A>C
|
XP_011530084.1:p.Asp1563Ala
|
|
XM_011531783.1:c.4466A>C
|
XP_011530085.1:p.Asp1489Ala
|
|
XM_017007925.1:c.4628A>C
|
XP_016863414.1:p.Asp1543Ala
|
|
XM_017007926.1:c.4625A>C
|
XP_016863415.1:p.Asp1542Ala
|
|
XM_024453956.1:c.4688A>C
|
XP_024309724.1:p.Asp1563Ala
|
|
XM_024453957.1:c.4685A>C
|
XP_024309725.1:p.Asp1562Ala
|
|
XM_024453958.1:c.2753A>C
|
XP_024309726.1:p.Asp918Ala
|
|
NM_001131007.2:c.4631A>C
MANE Select
|
NP_001124479.1:p.Asp1544Ala
|
|
NM_015196.4:c.4628A>C
|
NP_056011.3:p.Asp1543Ala
|
|