ENST00000254108.12:c.540T>A
MANE Select
|
ENSP00000254108.8:p.Asp180Glu
|
|
ENST00000254108.11:c.540T>A
|
ENSP00000254108.7:p.Asp180Glu
|
|
ENST00000380244.7:c.537T>A
|
ENSP00000369594.3:p.Asp179Glu
|
|
ENST00000487509.6:n.605T>A
|
|
|
ENST00000566605.5:c.540T>A
|
ENSP00000455073.1:p.Asp180Glu
|
|
ENST00000568685.1:c.540T>A
|
ENSP00000455282.1:p.Asp180Glu
|
|
NM_001170634.1:c.537T>A
|
NP_001164105.1:p.Asp179Glu
|
|
NM_001170937.1:c.528T>A
|
NP_001164408.1:p.Asp176Glu
|
|
NM_004960.3:c.540T>A , LRG_655t1:c.540T>A
|
NP_004951.1:p.Asp180Glu
|
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NR_028388.2:n.645T>A
|
|
|
XM_005255233.3:c.-41T>A
|
XP_005255290.1:n.-41T>A
|
|
XM_011545781.1:c.534T>A
|
XP_011544083.1:p.Asp178Glu
|
|
XM_011545782.1:c.-41T>A
|
XP_011544084.1:n.-41T>A
|
|
XM_005255233.5:c.-41T>A
|
XP_005255290.1:n.-41T>A
|
|
XM_011545782.2:c.-41T>A
|
XP_011544084.1:n.-41T>A
|
|
XM_024450221.1:c.531T>A
|
XP_024305989.1:p.Asp177Glu
|
|
NM_004960.4:c.540T>A
MANE Select
|
NP_004951.1:p.Asp180Glu
|
|